Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations

Description

The MECP2 gene is mutated in Rett syndrome (RTT ), a severe neurodevelopmental disorder that almost always occurs in females. Although it was first thought that MECP2 mutations causing Rett syndrome were lethal in males, later reports identified a severe neonatal encephalopathy in surviving male sibs of patients with Rett syndrome. Since then, additional reports have confirmed a severe phenotype in males with RTT-associated MECP2 mutations (Moog et al., 2003; Villard, 2007).Males with non-RTT mutations in the MECP2 gene can demonstrate a wide variety of phenotypes: see also nonspecific X-linked mental retardation, X-linked mental retardation with spasticity (OMIM ), and X-linked mental retardation due to increased dosage of the MECP2 gene (OMIM ).

Clinical Features

Top most frequent phenotypes and symptoms related to Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly
  • Growth delay
  • Failure to thrive
  • Nevus
  • Feeding difficulties
  • Hyperreflexia
  • Intellectual disability, severe
And another 24 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMet®Plus aCGH Analysis.

By Baylor Miraca Genetics Laboratories in United States.

GSN, NEFH, SOD1, TEAD1, PHB, PLA2G2A, AKAP10, PNKD, PAX2, CPOX, ABCB7, TAZ, TIMM8A, GK, PDHA1, HCCS, NYX, FRMD7, OTC, RP2 , (...)

View the complete list with 617 more genes
Specificity
1 %
Genes
100 %
MECP2 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Deletion/Duplication Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequence Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
PreSeek Non-invasive Prenatal Gene Sequencing Screen.

By Baylor Miraca Genetics Laboratories in United States.

NSD1, NIPBL, TSC1, SMC1A, SMC3, SYNGAP1, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
100 %
GeneAware Complete Panel Version 2 (Female).

By Baylor Miraca Genetics Laboratories in United States.

TMEM216, DPYD, TGM1, RAPSN, PKHD1, PLA2G6, PHGDH, LAMC2, EIF2B5, CLN5, CAPN3, BTK, ABCC8, WAS, TTPA, SUMF1, SLC17A5, SLC12A6, SGCG, RTEL1 , (...)

View the complete list with 139 more genes
Specificity
1 %
Genes
100 %
Complete Rett Syndrome Evaluation.

By Athena Diagnostics Inc in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (MECP2) Duplication/Deletion Test.

By Athena Diagnostics Inc in United States.

MECP2
Specificity
100 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc in United States.

IQSEC2, ATRX, SMS, OFD1, SERPINI1, KIF1BP, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, KCNJ10, SAMHD1, PNKP, SPTAN1, PLCB1, ANKRD11, PIGV, PIGN, DYRK1A , (...)

View the complete list with 214 more genes
Specificity
1 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation-Epileptic Encephalopathy.

By Athena Diagnostics Inc in United States.

TREX1, ZEB2, ARHGEF9, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, SAMHD1, PNKP, SPTAN1, PLCB1, PIGN, GRIN1, NRXN1, PIGA, SCN8A, WDR45, GNAO1, SZT2 , (...)

View the complete list with 47 more genes
Specificity
2 %
Genes
100 %
Epilepsy Advanced Sequencing and CNV Evaluation - Intellectual Disability.

By Athena Diagnostics Inc in United States.

GFAP, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, SYN1, KDM5C, PAK3, ARHGEF9, GRIA3, SYP, PHF6, FGD1, IQSEC2, ATRX, SMS, OFD1, DYRK1A, WDR45 , (...)

View the complete list with 36 more genes
Specificity
2 %
Genes
100 %
MECP2 Sequencing and CNV Evaluation.

By Athena Diagnostics Inc in United States.

MECP2
Specificity
100 %
Genes
100 %
Syndromic Autism Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

NLGN3, NLGN4X, CTNNB1, UBE3C, ARID1B, TMEM231, TBR1, HOXA1, CHD8, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2, KIRREL3, LAMC3, MED12, MID1, NTNG1, ADNP , (...)

View the complete list with 63 more genes
Specificity
2 %
Genes
100 %
NGS XLID Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

THOC2, CNKSR2, CDK16, CCDC22, CLCN4, FRMPD4, ZMYM3, ZCCHC12, WDR13, FAAH2, EIF2S3, LAS1L, GSPT2, KLF8, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, NAA10, SOX3 , (...)

View the complete list with 94 more genes
Specificity
1 %
Genes
100 %
Rett-Angelman Syndrome 2nd-Tier Sequencing Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

CTNNB1, EHMT1, ZEB2, OPHN1, ATRX, CNTNAP2, TCF4, PNKP, NRXN1, PQBP1, MBD5, FOLR1, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %
NGS Epilepsy/Seizure Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ATR, PCNT, FLVCR2, CDK5RAP2, GLI2, CDON, FOXH1, NODAL, ABCB1, CEP152, NALCN, ZIC2, TGIF1, TUBB2A, TSEN2, TSEN34, EXOSC3, KCNAB1, VANGL1, MTOR , (...)

View the complete list with 125 more genes
Specificity
1 %
Genes
100 %
Rett syndrome.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

MECP2
Specificity
100 %
Genes
100 %
Hereditary Spastic Paraplegia Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ZFYVE27, AP4M1, AP4E1, AP4B1, AP4S1, RAB3GAP2, ERLIN2, VPS37A, ADAR, DDHD1, TECPR2, DDHD2, CYP2U1, GBA2, TUBB4A, B4GALNT1, UCHL1, C19orf12, KIF1C, NT5C2 , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
100 %
Rett Syndrome.

By Center for Human Genetics, Inc in United States.

MECP2
Specificity
100 %
Genes
100 %
Autism Spectrum Disorders 53-Gene Panel.

By Center for Human Genetics, Inc in United States.

CNTNAP5, DLGAP2, DPP10, DPP6, GRPR, PCDH9, SLC9A9, ASTN2, CADM1, CNTN4, CXCR3, FABP5, FABP7, FBXO40, GLRA2, HNRNPH2, MBD1, MBD3, MBD4, MDGA2 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
100 %
MECP2-Related Disorders.

By Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 deletion/duplication.

By Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome, MECP2, Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome, MECP2, Sequencing and Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome, MECP2, Sequencing.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MECP2
Specificity
100 %
Genes
100 %
Autsim Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

NR1I3, AVPR1A, BDNF, SLC6A4, AUTS2, DOCK4, GABRG1, GNA14, IMMP2L, KATNAL2, KCTD13, KLHL3, NEGR1, PDE10A, PIP5K1B, PON3, SATB2, SMG6, SOX5, ST7 , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
Childhood Epilepsy.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

ZEB2, SYN1, CNTNAP2, PNKP, NRXN1, WDR45, MAGI2, MFSD8, TBC1D24, MBD5, GRIN2A, GABRG2, GABRA1, EPM2A, CHRNA4, CHRNA2, FOLR1, SCN2A, SCN1B, PRICKLE1 , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
100 %
Comprehensive Brain Malformation Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

DISP1, VLDLR, MYCN, RBBP8, IER3IP1, RAB18, PIK3CA, GAS1, EOMES, DLL1, ARL13B, CPLANE1, CEP41, KIF7, RPGRIP1L, TCTN1, TCTN2, TMEM138, TMEM237, TTC21B , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
100 %
Epilepsy/Seizure.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PSPH, PCBD1, ZEB2, CASK, OPHN1, SYN1, ARHGEF9, CNTNAP2, KCNJ10, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, WDR45, MAGI2, MFSD8, DNAJC5, ADGRG1, PAFAH1B1 , (...)

View the complete list with 78 more genes
Specificity
2 %
Genes
100 %
Infantile Epilepsy.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PCBD1, ZEB2, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, NRXN1, SCN8A, WDR45, MAGI2, MFSD8, PRRT2, TBC1D24, MBD5, GRIN2A, GABRG2, PNPO, KCNQ3, KCNQ2 , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
100 %
Microcephaly.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MYCN, RBBP8, IER3IP1, RAB18, RAB3GAP2, ATR, PCNT, CDK5RAP2, CEP152, ZEB2, CASK, ATRX, TCF4, STIL, RAB3GAP1, CENPJ, ASPM, MCPH1, NIPBL, WDR62 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
100 %
Rett - Angelman Syndrome.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

ZEB2, CNTNAP2, TCF4, NRXN1, WDR45, MBD5, MEF2C, FOXG1, CDKL5, SLC9A6, MECP2, UBE3A
Specificity
9 %
Genes
100 %
X-Linked Intellectual Disabilities Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PGK1, CNKSR2, CCDC22, FRMPD4, IL1RAPL1, NSDHL, NAA10, SOX3, SLC16A2, CLIC2, BRWD3, ZDHHC9, RPL10, RBM10, SHROOM4, RPS6KA3, FTSJ1, GDI1, ZDHHC15, UPF3B , (...)

View the complete list with 68 more genes
Specificity
2 %
Genes
100 %
X-linked Intellectual Disabilities Sequencing.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PGK1, CNKSR2, CCDC22, FRMPD4, IL1RAPL1, NSDHL, NAA10, SOX3, SLC16A2, CLIC2, BRWD3, ZDHHC9, RPL10, RBM10, SHROOM4, RPS6KA3, FTSJ1, GDI1, ZDHHC15, UPF3B , (...)

View the complete list with 68 more genes
Specificity
2 %
Genes
100 %
X-Linked Intellectual Disabilities Sequencing and Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PGK1, CNKSR2, CCDC22, FRMPD4, IL1RAPL1, NSDHL, NAA10, SOX3, SLC16A2, CLIC2, BRWD3, ZDHHC9, RPL10, RBM10, SHROOM4, RPS6KA3, FTSJ1, GDI1, ZDHHC15, UPF3B , (...)

View the complete list with 67 more genes
Specificity
2 %
Genes
100 %
MECP2 related disorders.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequencing, Family-targeted (Single Exon Sequencing - Known Mutation).

By Molecular Diagnostic Laboratory LabCorp in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequencing, Full Gene.

By Molecular Diagnostic Laboratory LabCorp in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Deletion/Duplication Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 related disorders-RETT syndrome.

By Genetics Laboratory University of Oklahoma Health Sciences Center in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett/Angelman Syndrome Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

EHMT1, ZEB2, OPHN1, ATRX, CNTNAP2, TCF4, PNKP, DYRK1A, NRXN1, MBD5, FOLR1, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
5 %
Genes
100 %
MECP2 sequencing.

By Genetic Services Laboratory University of Chicago in United States.

MECP2
Specificity
100 %
Genes
100 %
Non-Specific Intellectual Disability Panel.

By Genetic Services Laboratory University of Chicago in United States.

CA8, CC2D1A, CRBN, GRIK2, MAN1B1, PRSS12, TRAPPC9, ZC3H14, ZNF526, ZNF674, CDH15, SOBP, C12orf57, LINS1, LRP2, MED23, SLC25A1, KPTN, PACS1, VLDLR , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
100 %
X-linked Non-Specific Intellectual Disability Panel.

By Genetic Services Laboratory University of Chicago in United States.

ZNF674, CCDC22, FRMPD4, EIF2S3, KLF8, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, NAA10, SLC16A2, CLIC2, BRWD3, ZDHHC9, RPL10, SHROOM4, RPS6KA3, FTSJ1, GDI1, ZDHHC15 , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
100 %
Angelman Syndrome Tier 2 Panel.

By Genetic Services Laboratory University of Chicago in United States.

TCF4, SLC9A6, MECP2, UBE3A
Specificity
25 %
Genes
100 %
Rett/Atypical Rett Syndrome Panel.

By Genetic Services Laboratory University of Chicago in United States.

MEF2C, FOXG1, CDKL5, MECP2
Specificity
25 %
Genes
100 %
Rett/Angelman Syndrome Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

TRAPPC9, EHMT1, ZEB2, OPHN1, ATRX, CNTNAP2, TCF4, PNKP, DYRK1A, NRXN1, WDR45, MBD5, FOLR1, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
100 %
MECP2 deletion/duplication analysis.

By Genetic Services Laboratory University of Chicago in United States.

MECP2
Specificity
100 %
Genes
100 %
Microcephaly Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

TUBGCP6, ASXL3, TUBGCP4, PYCR2, CRIPT, PLK4, ORC4, ORC6, CDT1, CDC6, ORC1, TRAPPC9, CEP63, KNL1, CEP135, ZNF335, CDK6, PHC1, CENPE, MFSD2A , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
100 %
Microcephaly Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

SLC1A4, PPP1R15B, USP18, TUBGCP6, ASXL3, TUBGCP4, PYCR2, CRIPT, PLK4, ORC4, ORC6, CDT1, CDC6, ORC1, NIN, TRAPPC9, CEP63, KNL1, CEP135, ZNF335 , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
100 %
Dystonia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

NUP62, ACY1, SLC30A10, ADCY5, GNAL, BCAP31, ECHS1, LIPT1, KCTD17, HPCA, XPR1, ANO3, HIVEP2, GNB1, DNAJC6, SLC39A14, VAC14, UBA5, TBCD, MECR , (...)

View the complete list with 150 more genes
Specificity
1 %
Genes
100 %
Ataxia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

PIGG, CHAMP1, THG1L, VWA3B, CWF19L1, WDR73, TMEM240, SNX14, APOPT1, CHCHD10, PRDM8, PET100, RNF170, POLR3B, POLR3A, WDR81, COA5, ZNF592, XPA, TRNT1 , (...)

View the complete list with 460 more genes
Specificity
1 %
Genes
100 %
Rett Syndrome.

By United States Air Force Molecular Diagnostic Laboratory United States Air Force in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome.

By Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital in New Zealand.

MECP2
Specificity
100 %
Genes
100 %
RETT syndrome (MECP2).

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

MECP2
Specificity
100 %
Genes
100 %
Epilepsy Panel - Comprehensive.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

PSAT1, CERS1, PSPH, NECAP1, NEU1, ZEB2, CNTNAP2, TCF4, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, DOCK7, DNM1, PRRT2, TBC1D24, ASAH1, SCARB2, MBD5 , (...)

View the complete list with 49 more genes
Specificity
2 %
Genes
100 %
RETT SYNDROME; RTT.

By Human Genetics Ruhr University in Germany.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (MECP2), Full Gene Analysis.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (MECP2), Full Gene Sequencing.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (MECP2), Deletion and Duplication.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MECP2
Specificity
100 %
Genes
100 %
Comprehensive Epilepsy Panel.

By GeneDx in United States.

ZEB2, ATP6AP2, SYN1, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, NRXN1, SCN8A, KANSL1, MAGI2, MFSD8, DNAJC5, SRPX2, PRRT2, TBC1D24, SCARB2, MBD5, GRIN2A , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
100 %
STAT Epilepsy Panel.

By GeneDx in United States.

SPTAN1, SCN8A, PNPO, KCNQ3, KCNQ2, FOLR1, SCN2A, SCN1B, SCN1A, SLC2A1, PCDH19, MEF2C, CDKL5, ARX, ALDH7A1, STXBP1, MECP2, POLG
Specificity
6 %
Genes
100 %
Infantile Epilepsy Panel.

By GeneDx in United States.

ZEB2, ATP6AP2, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, NRXN1, SCN8A, KANSL1, MAGI2, MFSD8, PRRT2, TBC1D24, MBD5, GRIN2A, GABRG2, GABRA1, PNPO, KCNQ3 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
100 %
Childhood-Onset Epilepsy Panel.

By GeneDx in United States.

ZEB2, SYN1, CNTNAP2, TCF4, PNKP, NRXN1, KANSL1, MAGI2, MFSD8, TBC1D24, MBD5, GRIN2A, GABRG2, GABRA1, EPM2A, CHRNA4, CHRNA2, FOLR1, SCN2A, SCN1B , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
100 %
Rett/Angelman Syndrome Panel.

By GeneDx in United States.

ZEB2, CNTNAP2, TCF4, NRXN1, MBD5, MEF2C, FOXG1, CDKL5, SLC9A6, MECP2, UBE3A
Specificity
10 %
Genes
100 %
Rett Syndrome.

By Molecular Diagnostics Lab Nemours Alfred I. duPont Hospital for Children in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Duplication Syndrome.

By Molecular Diagnostics Lab Nemours Alfred I. duPont Hospital for Children in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett/Atypical Rett/Angelman.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

EHMT1, ZEB2, ATRX, CNTNAP2, TCF4, PNKP, NRXN1, MBD5, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
7 %
Genes
100 %
Autism/Intellectual Disability/Multiple Anomalies.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

ERCC8, RPGRIP1L, AVPR1A, BDNF, SLC6A4, ERCC6, SPRED1, RPS6KA3, NLGN3, NLGN4X, HOXA1, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, SHANK2, SHANK3 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
AutismNext.

By Ambry Genetics in United States.

POGZ, KATNAL2, UPF3B, NLGN3, NLGN4X, ARID1B, TBR1, CHD8, CACNA1C, FOXP1, MED12, ADNP, PTCHD1, SHANK3, ZEB2, RAB39B, GRIA3, CNTNAP2, TCF4, ANKRD11 , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
100 %
CustomNext: Neuro.

By Ambry Genetics in United States.

KAT6A, DDX3X, POGZ, CA8, CC2D1A, MAN1B1, TRAPPC9, LINS1, MED23, CTCF, PACS1, KATNAL2, SATB2, AP4B1, SMARCA2, SMARCB1, SMARCA4, NSUN2, SLC16A2, BRWD3 , (...)

View the complete list with 176 more genes
Specificity
1 %
Genes
100 %
MECP2 gene sequence and deletion/duplication.

By Ambry Genetics in United States.

MECP2
Specificity
100 %
Genes
100 %
Neurodevelopment-Expanded.

By Ambry Genetics in United States.

KAT6A, DDX3X, POGZ, CA8, CC2D1A, MAN1B1, TRAPPC9, LINS1, MED23, CTCF, PACS1, KATNAL2, SATB2, AP4B1, SMARCA2, SMARCB1, SMARCA4, NSUN2, SLC16A2, BRWD3 , (...)

View the complete list with 176 more genes
Specificity
1 %
Genes
100 %
EpilepsyNext.

By Ambry Genetics in United States.

ZEB2, CASK, SYN1, ARHGEF9, IQSEC2, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, PLCB1, DYRK1A, GRIN1, NRXN1, PIGA, SCN8A, ST3GAL3, WDR45, GNAO1, SZT2 , (...)

View the complete list with 80 more genes
Specificity
1 %
Genes
100 %
EpiRapid.

By Ambry Genetics in United States.

SCN8A, PRRT2, PNPO, KCNQ3, KCNQ2, KCNT1, FOLR1, SCN1A, TSC1, TSC2, SLC2A1, PCDH19, ALDH7A1, STXBP1, MECP2, POLG
Specificity
7 %
Genes
100 %
EpiRapid reflex EpilepsyNext.

By Ambry Genetics in United States.

ZEB2, CASK, SYN1, ARHGEF9, IQSEC2, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, PLCB1, DYRK1A, GRIN1, NRXN1, PIGA, SCN8A, ST3GAL3, WDR45, GNAO1, SZT2 , (...)

View the complete list with 80 more genes
Specificity
1 %
Genes
100 %
IDNext.

By Ambry Genetics in United States.

KAT6A, DDX3X, CA8, CC2D1A, MAN1B1, TRAPPC9, LINS1, MED23, CTCF, PACS1, SATB2, AP4B1, SMARCA2, SMARCB1, SMARCA4, NSUN2, SLC16A2, BRWD3, RPL10, RPS6KA3 , (...)

View the complete list with 120 more genes
Specificity
1 %
Genes
100 %
MECP2 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

MECP2
Specificity
100 %
Genes
100 %
MECP2, SCN1B, GABRG2, LGI1, POLG, POLG2, SLC25A22, SPTAN1, SRPX2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SPTAN1, SRPX2, GABRG2, SCN1B, LGI1, SLC25A22, POLG2, MECP2, POLG
Specificity
12 %
Genes
100 %
MECP2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MECP2
Specificity
100 %
Genes
100 %
MECP2. MLPA testing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MECP2
Specificity
100 %
Genes
100 %
MECP2, NTNG1, CDKL5. NextGeneDx. Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

NTNG1, CDKL5, MECP2
Specificity
34 %
Genes
100 %
Rett syndrome.

By Molecular Diagnostics Laboratory Hospital Sainte-Justine in Canada.

MECP2
Specificity
100 %
Genes
100 %
Infantile Spasms/Atypical Rett Panel - MECP2, ARX, CDKL5 Sequence and Del/Dup Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

CDKL5, ARX, MECP2
Specificity
34 %
Genes
100 %
Rett Syndrome - MECP2 Sequence and Del/Dup Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome - MECP2 Sequence Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome - MECP2 Deletion/Duplication Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome - MECP2 Known Point Mutation Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

MECP2
Specificity
100 %
Genes
100 %
Angelman/Rett Seq.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

EHMT1, ZEB2, OPHN1, ATRX, TCF4, PNKP, DYRK1A, MBD5, FOLR1, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
6 %
Genes
100 %
Angelman/Rett Del/Dup.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

EHMT1, ZEB2, OPHN1, ATRX, TCF4, PNKP, DYRK1A, MBD5, FOLR1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
6 %
Genes
100 %
CHOP Epilepsy Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

PIGT, SLC12A5, HDAC4, CNKSR2, ZEB2, CASK, SYN1, ARHGEF9, IQSEC2, KCNJ10, PNKP, SPTAN1, PLCB1, GRIN1, PIGA, SCN8A, ST3GAL3, WDR45, GNAO1, SZT2 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Angelman/ Rett Seq + Del/Dup.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

EHMT1, ZEB2, OPHN1, ATRX, TCF4, PNKP, DYRK1A, MBD5, FOLR1, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
6 %
Genes
100 %
MECP2 Gene Deletion/Duplication Analysis.

By Molecular Genetics Laboratory Children's Mercy Hospital and Clinics in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Gene Sequence Analysis.

By Molecular Genetics Laboratory Children's Mercy Hospital and Clinics in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 duplication syndrome.

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
X-Linked Syndromic Mental Retardation 13.

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
MECP2-Related Angelman-like Syndrome.

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome (sequence and deletion/duplication analysis of MECP2 gene).

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (deletion/duplication analysis of MECP2 gene).

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome (sequence analysis of MECP2 gene).

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Mental retardation, X-linked syndromic, Lubs type (deletion/duplication analysis of MECP2).

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Encephalopathy (deletion/duplication analysis of MECP2 gene).

By CGC Genetics in Portugal.

MECP2
Specificity
100 %
Genes
100 %
Psychomotor development delay (various syndromes, deletion/duplication analysis).

By CGC Genetics in Portugal.

NF1, MECP2
Specificity
50 %
Genes
100 %
Epileptic encephalopathy (NGS panel for 67 genes).

By CGC Genetics in Portugal.

SRGAP2, MAPK10, ACY1, TBCE, TREX1, ZEB2, ARHGEF9, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, KCNJ10, SAMHD1, PNKP, SPTAN1, PLCB1, GRIN1, NRXN1, SCN8A , (...)

View the complete list with 47 more genes
Specificity
2 %
Genes
100 %
Mental retardation, X-linked (NGS panel for 89 genes).

By CGC Genetics in Portugal.

KIF4A, MID2, PGK1, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, SOX3, SLC16A2, CLIC2, BRWD3, ZDHHC9, SHROOM4, RPS6KA3, FTSJ1, GDI1, USP9X, UPF3B, UBE2A, TSPAN7 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Dystonia (NGS panel for 43 genes).

By CGC Genetics in Portugal.

CACNA1B, SLC30A10, GNAL, BCAP31, KCTD17, HPCA, ANO3, PRKRA, SLC6A3, DRD2, MR1, DDC, FTL, TUBB4A, TAF1, ACTB, VPS13A, PRRT2, KCNMA1, ATP1A3 , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
100 %
Rett and Rett-like syndrome (NGS panel of 8 genes).

By CGC Genetics in Portugal.

IQSEC2, TCF4, KCNA2, MBD5, MEF2C, FOXG1, CDKL5, MECP2
Specificity
13 %
Genes
100 %
Rett and Rett-like syndrome (NGS panel of 8 genes).

By CGC Genetics in Portugal.

IQSEC2, TCF4, KCNA2, MBD5, MEF2C, FOXG1, CDKL5, MECP2
Specificity
13 %
Genes
100 %
MECP2-Related Disorders.

By Laboratory of Genetics HUSLAB in Finland.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome.

By Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital in India.

MECP2
Specificity
100 %
Genes
100 %
Early Infantile Epileptic Encephalopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TNK2, NPRL2, ACY1, ARHGEF9, CNTNAP2, KCNJ10, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, ROGDI, ST3GAL3, GNAO1, SZT2, SLC13A5, KCNB1, KCNA2, MFSD8, CTSF , (...)

View the complete list with 62 more genes
Specificity
2 %
Genes
100 %
Rett Syndrome via the MECP2 Gene.

By PreventionGenetics PreventionGenetics in United States.

MECP2
Specificity
100 %
Genes
100 %
Comprehensive Epilepsy and Seizure Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CARS2, KCNH1, SLC1A2, PLPBP, SON, RORB, HCN2, GRIN2D, FRRS1L, CAD, NACC1, TNK2, NPRL2, NPRL3, SCN10A, PIGG, ACY1, GNB1, TUBG1, IER3IP1 , (...)

View the complete list with 133 more genes
Specificity
1 %
Genes
100 %
X-Linked Intellectual Disability Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

USP27X, SYTL5, KLHL15, MAP7D3, SLC7A3, MAGEA11, RLIM, DRP2, MSL3, NONO, H2BFWT, ARSF, RNF113A, HMGB3, SSR4, DDX3X, POLA1, KCNE5, BCAP31, KIF4A , (...)

View the complete list with 108 more genes
Specificity
1 %
Genes
100 %
Non-syndromic Intellectual Disability (NS-ID) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DCPS, MYT1L, MED13L, TRIO, SIN3A, MAP3K7, ELP2, EXTL3, CIC, TBC1D23, TRAPPC6B, ABI2, CAPS, DMBT1, FBXO47, MAPK8, PIDD1, SDK2, SLAIN1, SPATA13 , (...)

View the complete list with 90 more genes
Specificity
1 %
Genes
100 %
Autism Spectrum Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MBD6, WDFY3, DGAT2L6, CDC42BPB, SYN2, STXBP5, KAT2B, TNRC6B, TCF20, KMT5B, MYO9B, CSMD1, NAA15, DSCAM, DISC1, EFR3A, CTTNBP2, CNTN6, CTNND2, ASH1L , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
Rett Syndrome, Angelman Syndrome and Variant Syndromes Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ZEB2, CNTNAP2, TCF4, NRXN1, WDR45, MBD5, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
8 %
Genes
100 %
Epilepsy and Seizure Plus Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DENND5A, RBFOX3, HECW2, GUF1, KPNA7, STRADA, RAB11A, NUS1, ITPA, CNTN2, SNX27, ARHGEF15, PPP3CA, PIK3AP1, JMJD1C, AP3B2, FASN, YWHAG, KCND2, RYR3 , (...)

View the complete list with 202 more genes
Specificity
1 %
Genes
100 %
Mental retardation - different panels.

By Institute of Human Genetics Cologne University in Germany.

EEF1B2, UBR7, PARP1, CAPN10, SLC31A1, TRMT1, PGAP2, GMPPA, TANGO2, IMPA1, RALGDS, ZBTB40, KCNK9, SETD1A, HERC2, TM4SF20, AHDC1, CCDC88A, ACBD6, KDM5A , (...)

View the complete list with 847 more genes
Specificity
1 %
Genes
100 %
Rett Syndrome, Congenital Variant.

By MGZ Medical Genetics Center in Germany.

MECP2
Specificity
100 %
Genes
100 %
MECP2-Related Disorders.

By MGZ Medical Genetics Center in Germany.

MECP2
Specificity
100 %
Genes
100 %
Neurogenetic Disorders - panels.

By MGZ Medical Genetics Center in Germany.

PITRM1, KLC4, PTCD1, VPS11, TXN2, STAT2, PODXL, PPT2, GTPBP2, SLC25A26, KCNA4, SLC25A42, FLRT1, CCDC115, TANGO2, LONP1, TRIT1, RMND1, VARS2, TARS2 , (...)

View the complete list with 577 more genes
Specificity
1 %
Genes
100 %
Mental Retardation and Dysmorphology - panels.

By MGZ Medical Genetics Center in Germany.

GATAD2B, CUL7, SPECC1L, IRF6, CCNQ, ROR2, CCND2, HEPACAM, TBC1D7, KPTN, WNT5A, SRCAP, UBR1, C2CD3, TCTN3, NOTCH2, PACS1, EPG5, ERCC8, AKT1 , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
100 %
Syndromal Diseases - panels.

By MGZ Medical Genetics Center in Germany.

PACS1, EPG5, ERCC8, AKT1, AKT3, PIK3R2, INSR, IDH1, ALX1, GNAQ, PIK3CA, CPLANE1, KIF7, GNAS, TRIM37, EFTUD2, EFNB1, EP300, TBX5, SALL4 , (...)

View the complete list with 322 more genes
Specificity
1 %
Genes
100 %
Epileptic Encephalopathy.

By MGZ Medical Genetics Center in Germany.

PPT2, ARHGEF15, CLP1, GPHN, KCNH5, IBA57, HADH, DCAF17, CP, FTL, C19orf12, HNRNPDL, TUBB2A, CLCN4, NEU1, GFAP, ARHGEF9, PNKP, SPTAN1, PLCB1 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Epileptic Encephalopathy – Basic Diagnostics.

By MGZ Medical Genetics Center in Germany.

GABRA1, PNPO, KCNC1, KCNQ2, KCNT1, HCN1, FOLR1, SCN2A, SCN1A, PHGDH, PPT1, SYNGAP1, SLC2A1, PCDH19, FOXG1, CDKL5, ARX, ALDH7A1, STXBP1, GAMT , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
X-Linked Mental Retardation.

By MGZ Medical Genetics Center in Germany.

NXF5, FAM126A, ZNF674, PGK1, CTDP1, GAN, KDM6A, THOC2, CLCN4, ZMYM3, EIF2S3, LAS1L, KLF8, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, NAA10, SOX3, SLC16A2 , (...)

View the complete list with 93 more genes
Specificity
1 %
Genes
100 %
Epilepsy and Mitochondrial Encephalopathy.

By MGZ Medical Genetics Center in Germany.

PTCD1, PPT2, RMND1, VARS2, TARS2, ARHGEF15, FLAD1, LYRM7, NDUFB9, CLP1, UQCRC2, GPHN, SERAC1, KCNH5, IBA57, MICU1, EIF2AK3, HADH, EARS2, TPK1 , (...)

View the complete list with 166 more genes
Specificity
1 %
Genes
100 %
Brain Malformations / Neuronal Migration Disorders.

By MGZ Medical Genetics Center in Germany.

NXF5, HERC2, ARHGEF15, JAM3, DARS, CLP1, DIS3L2, COL4A2, POLR3B, POLR3A, ITM2B, STUB1, NOL3, SEPSECS, KCNH5, ZNF674, KIF2A, KIF5C, TUBB, TUBG1 , (...)

View the complete list with 246 more genes
Specificity
1 %
Genes
100 %
Angelman Syndrome and Differential Diagnoses.

By MGZ Medical Genetics Center in Germany.

HERC2, EHMT1, ZEB2, KDM5C, ATRX, CNTNAP2, TCF4, DYRK1A, NRXN1, NEXMIF, MBD5, SYNGAP1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
5 %
Genes
100 %
Epilepsy.

By MGZ Medical Genetics Center in Germany.

PTCD1, PPT2, TRIT1, RMND1, VARS2, TARS2, ARHGEF15, FLAD1, LYRM7, NDUFB9, CLP1, UQCRC2, GPHN, FAM126A, POLR3B, POLR3A, NOL3, SERAC1, KCNH5, IBA57 , (...)

View the complete list with 192 more genes
Specificity
1 %
Genes
100 %
Rett syndrome.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

MECP2
Specificity
100 %
Genes
100 %
Epileptic encephalopathy panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

SRGAP2, MAPK10, TBCE, ZEB2, ARHGEF9, PNKP, SPTAN1, PLCB1, SCN8A, MAGI2, GRIN2A, PNPO, KCNQ2, KCNT1, GRIN2B, SCN2A, SCN1B, SLC19A3, SCN9A, SCN1A , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
100 %
Epileptic syndromes with epilepsy and intellectual disability panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

AUTS2, CNKSR2, MED12, TREX1, ZEB2, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, KDM5C, PAK3, GRIA3, SYP, PHF6, FGD1, ATRX, SMS, OFD1, CNTNAP2 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
100 %
Rett syndrome.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Angelman-like syndrome.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Mental retardation X-linked, syndromic, Lubs type.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Central hypoventilation syndrome, congenital.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Autism susceptibility, X-linked type 3.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Encephalopathy neonatal severe.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

FCGR2B, TNF, ALOX5AP, PRKCH, TLR5, TIRAP, NOS2, XBP1, KCNK18, AANAT, SNIP1, EIF4E, ZBTB18, ADAM10, YAP1, ICAM1, SNX3, CISH, TAS2R38, FRG1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
100 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
Mental retardation, X-Linked type 13.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome preserved speech variant.

By Centogene AG - the Rare Disease Company in Germany.

MECP2
Specificity
100 %
Genes
100 %
Autism Spectrum Disorders / Intellectual Disability.

By Michigan Medical Genetics Laboratories University of Michigan in United States.

MECP2, PTEN
Specificity
50 %
Genes
100 %
Rett syndrome.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

MECP2
Specificity
100 %
Genes
100 %
Epileptic Encephalopathy Panel.

By CeGaT GmbH in Germany.

GPHN, HDAC4, ACY1, ADAR, TREX1, ZEB2, CASK, SYN1, ARHGEF9, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, SAMHD1, PNKP, SPTAN1, PLCB1, GRIN1, NRXN1 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
100 %
Epilepsy and X-linked Mental Retardation with Seizures Panel.

By CeGaT GmbH in Germany.

PGK1, UBE2A, MED12, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, SYN1, KDM5C, PAK3, ARHGEF9, GRIA3, SYP, PHF6, IQSEC2, ATRX, SMS, OFD1, PCDH19 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
100 %
Hereditary Degenerative Syndromes Panel.

By CeGaT GmbH in Germany.

DRD1, NUP62, SLC30A10, HEPACAM, SLC6A3, FBXO7, CSF1R, FTL, JPH3, C19orf12, SLC16A2, TAF1, FUCA1, VPS13A, WDR45, ATP13A2, ARFGEF2, DCTN1, ATN1, TBP , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
100 %
Dystonia All Panel.

By CeGaT GmbH in Germany.

MED20, CACNA1B, CIZ1, ACY1, SLC30A10, ADCY5, GNAL, BCAP31, KCTD17, HPCA, ANO3, COX20, PRKRA, CSF1R, FTL, TUBB4A, KIF1C, TAF1, VPS13A, PRRT2 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
100 %
Test for MECP2-Related Disorders.

By All Wales Genetics Laboratory Institute of Medical Genetics in United Kingdom.

MECP2
Specificity
100 %
Genes
100 %
MECP2-Related Disorders.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

MECP2
Specificity
100 %
Genes
100 %
Angelman syndrome (MECP2).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

MECP2
Specificity
100 %
Genes
100 %
METHYL-CpG-BINDING PROTEIN 2.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

MECP2
Specificity
100 %
Genes
100 %
METHYL-CpG-BINDING PROTEIN 2.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

MECP2
Specificity
100 %
Genes
100 %
Epilepsy.

By Asper Biogene Asper Biogene LLC in Estonia.

SNIP1, ITPA, GPHN, PIGT, SLC12A5, CERS1, FGF12, KIF5C, ADAR, SMARCA2, AARS, MTOR, NECAP1, ZDHHC9, HUWE1, CACNA1D, CASK, ATP6AP2, SYN1, ARHGEF9 , (...)

View the complete list with 104 more genes
Specificity
1 %
Genes
100 %
Brain malformations.

By Asper Biogene Asper Biogene LLC in Estonia.

CLP1, TUBGCP6, SEPSECS, AMPD2, CEP63, KNL1, CEP135, LAMB1, SNAP29, ERMARD, KIF2A, KIF5C, TUBB, TUBG1, RTTN, TBC1D20, CCND2, ZNF423, OCLN, TCTN3 , (...)

View the complete list with 125 more genes
Specificity
1 %
Genes
100 %
Autism Spectrum Disorders.

By Asper Biogene Asper Biogene LLC in Estonia.

EN2, PDE8B, AVPR1A, SLC6A4, SLC9A9, MAGEL2, RPL10, NLGN4X, HOXA1, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, NTNG1, ADNP, PTCHD1, SHANK3, VPS13B , (...)

View the complete list with 32 more genes
Specificity
2 %
Genes
100 %
MECP2-Related Disorders.

By Labor-MVZ Westmecklenburg Laboratory for Molecular Diagnostics in Germany.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Duplication Syndrome.

By Labor-MVZ Westmecklenburg Laboratory for Molecular Diagnostics in Germany.

MECP2
Specificity
100 %
Genes
100 %
MECP2-Related Disorders.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

MECP2
Specificity
100 %
Genes
100 %
Angelman syndrome.

By Praxis fuer Humangenetik Wien in Austria.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome.

By Praxis fuer Humangenetik Wien in Austria.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Gene Sequencing.

By GENETIX Centro de Investigación en Genética Humana y Reproductiva in Colombia.

MECP2
Specificity
100 %
Genes
100 %
MECP2.

By Division Human Genetics Medical University Innsbruck in Austria.

MECP2
Specificity
100 %
Genes
100 %
qChip.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

SEM1, IGF2, CBFB, TRAPPC10, FBXW11, TBX3, HDAC4, TRPS1, STS, HOXD13, LMNB1, MID2, IRF6, MNX1, SIM1, DISP1, MYCN, GATA4, ZIC3, VEGFA , (...)

View the complete list with 106 more genes
Specificity
1 %
Genes
100 %
qCarrier Plus.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

MPP3, FTCD, ADK, CTH, HAL, HGD, WNT10A, SLC6A19, TPO, SLC5A5, DUOX2, DUOXA2, PAX8, HJV, HOGA1, TFR2, COL7A1, SLC39A4, ARL13B, FANCA , (...)

View the complete list with 280 more genes
Specificity
1 %
Genes
100 %
Angelman syndrome.

By MedGene in Slovakia.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome.

By MedGene in Slovakia.

MECP2
Specificity
100 %
Genes
100 %
Invitae Epilepsy Panel.

By Invitae in United States.

ITPA, SNX27, FRRS1L, NGLY1, GLRA1, C12orf57, PACS1, IER3IP1, SATB2, ZDHHC9, EHMT1, ZEB2, CASK, SYN1, ARHGEF9, IQSEC2, ATRX, SERPINI1, CNTNAP2, TCF4 , (...)

View the complete list with 105 more genes
Specificity
1 %
Genes
100 %
Invitae Rett and Angelman Syndromes and Related Disorders Panel.

By Invitae in United States.

NGLY1, SATB2, EHMT1, ZEB2, IQSEC2, ATRX, CNTNAP2, TCF4, DYRK1A, NRXN1, SCN8A, KANSL1, MBD5, MEF2C, FOXG1, CDKL5, ALDH5A1, SLC9A6, STXBP1, MECP2 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
Rett syndrome: MECP2 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome: MECP2 gene deletions-duplications analysis (MLPA).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MECP2
Specificity
100 %
Genes
100 %
Mental retardation, X-linked, Lubs type: MECP2 gene duplications analysis (MLPA).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MECP2
Specificity
100 %
Genes
100 %
Epileptic encephalopathies.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MAPK10, AARS, TREX1, CASK, ARHGEF9, PNKP, SPTAN1, PLCB1, PIGA, SCN8A, ST3GAL3, DNM1, SRPX2, DCX, TBC1D24, MBD5, GRIN2A, GABRA1, CHD2, KCNQ2 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
100 %
Mental retardation, X-linked, non-syndromic.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

ZNF674, IL1RAPL1, ZNF81, ARHGEF6, BRWD3, SHROOM4, RPS6KA3, FTSJ1, GDI1, UPF3B, TSPAN7, DLG3, ZNF41, ZNF711, AFF2, AGTR2, HUWE1, NLGN4X, AP1S2, CASK , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
Autism.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

OXTR, GABRG3, GABRA5, EN2, PDE8B, LAMB1, SLC6A4, SLC9A9, CNTN4, RPL10, NLGN3, NLGN4X, HOXA1, CACNA1C, FOXP2, PTCHD1, SHANK3, CNTNAP2, NRXN1, RELN , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
100 %
Rett, Syndrome.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

HERC2, BDNF, FOXP1, FOXP2, NTNG1, SHANK3, TCF4, KCNQ2, SCN2A, PLP1, MEF2C, FOXG1, CDKL5, ARX, ALDH5A1, STXBP1, MECP2, UBE3A
Specificity
6 %
Genes
100 %
Rett Syndrome: MECP2 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome: MECP2 Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MECP2
Specificity
100 %
Genes
100 %
Epilepsy and Seizure Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ZEB2, CASK, ATP6AP2, OPHN1, SYN1, ARHGEF9, PHF6, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, ST3GAL3, MAGI2, MFSD8, DNAJC5, SRPX2 , (...)

View the complete list with 90 more genes
Specificity
1 %
Genes
100 %
X-linked Intellectual Disability: Gene Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

PGK1, CNKSR2, CDK16, CCDC22, FRMPD4, KLF8, IL1RAPL1, NSDHL, NAA10, SOX3, SLC16A2, CLIC2, BRWD3, ZDHHC9, RPL10, RBM10, SHROOM4, RPS6KA3, FTSJ1, GDI1 , (...)

View the complete list with 71 more genes
Specificity
2 %
Genes
100 %
Autism Spectrum Disorders: Tier 2 Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

NR1I3, SMARCB1, MAGEL2, UBE2A, AFF2, NLGN3, NLGN4X, CHD8, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, PTCHD1, VPS13B, ZEB2, RAB39B, CASK , (...)

View the complete list with 42 more genes
Specificity
2 %
Genes
100 %
Neurology: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MAPK10, POC1A, ORC4, ORC6, CDT1, CDC6, NIN, CEP63, KNL1, CEP135, ZNF335, RTTN, DISP1, VLDLR, MYCN, RBBP8, RAB18, EOMES, CEP41, KIF7 , (...)

View the complete list with 144 more genes
Specificity
1 %
Genes
100 %
Pan-Ethnic Carrier Screen: Gene Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

HMOX1, LIPH, NLRP7, EDAR, WISP3, WRN, GP9, TTC37, GP1BB, F9, VWF, F11, MEFV, CTSC, SLC19A2, VPS13B, CYP21A2, GHRHR, TMEM216, DPYD , (...)

View the complete list with 127 more genes
Specificity
1 %
Genes
100 %
Autism Spectrum Disorders: Tier 2 Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

NR1I3, SMARCB1, MAGEL2, UBE2A, AFF2, NLGN3, NLGN4X, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, PTCHD1, VPS13B, ZEB2, RAB39B, CASK, OPHN1 , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
100 %
Epilepsy and Seizure Disorders: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ZEB2, CASK, ATP6AP2, OPHN1, SYN1, ARHGEF9, PHF6, CNTNAP2, TCF4, KCNJ10, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, ST3GAL3, MAGI2, MFSD8, DNAJC5, SRPX2 , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
Autism NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

AVPR1A, BDNF, SLC6A4, AUTS2, DOCK4, GABRG1, GNA14, IMMP2L, KATNAL2, KCTD13, KLHL3, NEGR1, PDE10A, PIP5K1B, PON3, SATB2, SMG6, SOX5, ST7, STK3 , (...)

View the complete list with 80 more genes
Specificity
1 %
Genes
100 %
Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

EFHC2, CELSR1, GPHN, SLC6A5, GLRA1, GLRB, SCN10A, BUB1B, MAPK10, COL18A1, ACY1, MED17, SNAP29, LIG4, NHEJ1, SLC46A1, ARL13B, RPGRIP1L, PGK1, SCN4B , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
100 %
Intellectual Disability NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

AQP7, TPH2, AFP, XIST, SNIP1, ZBTB24, GLUL, DIP2B, KCNK9, UPB1, CEP57, FTO, ZBTB16, TMCO1, IRX5, AGT, IGF1R, MRAP, HDAC4, IGF1 , (...)

View the complete list with 372 more genes
Specificity
1 %
Genes
100 %
Migraine NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

PNPO, KCNQ2, FOLR1, ATP1A2, CACNA1A, SCN1A, PHGDH, PPT1, SLC2A1, PCDH19, FOXG1, CDKL5, ARX, ALDH7A1, STXBP1, GAMT, MECP2, POLG
Specificity
6 %
Genes
100 %
Rett-Angelman Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TRAPPC9, MED17, CAV1, ZEB2, OPHN1, ATRX, CNTNAP2, TCF4, PNKP, SLC2A1, PCDH19, MEF2C, FOXG1, CDKL5, ARX, SLC9A6, MECP2, UBE3A
Specificity
6 %
Genes
100 %
Nuclear-Mito NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CNR1, CHDH, CLYBL, NIPSNAP3A, IDE, IMMT, LETM1, MAVS, RAB11FIP5, POLRMT, PTGES2, PPARGC1A, AS3MT, ACSM3, ACSL5, DMAC2, ATP10D, NDUFB1, HK2, ECI1 , (...)

View the complete list with 484 more genes
Specificity
1 %
Genes
100 %
XLID NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

ZNF674, PGK1, CNKSR2, CCDC22, FRMPD4, ZCCHC12, WDR13, FAAH2, GSPT2, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, NAA10, SOX3, SLC16A2, TAF1, CLIC2, BRWD3, ZDHHC9 , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
MECP2.

By Fulgent Genetics Fulgent Genetics in United States.

MECP2
Specificity
100 %
Genes
100 %
Essential Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MAPK10, ACY1, TREX1, ZEB2, ARHGEF9, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, SAMHD1, PNKP, SPTAN1, PLCB1, NRXN1, SCN8A, ROGDI, ST3GAL3, GNAO1, SZT2 , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
100 %
Idiopathic Generalized Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

NIPA2, CNTN2, DHFR, CLCN2, ZEB2, RAB39B, CUL4B, CASK, ATP6AP2, OPHN1, SYN1, KDM5C, PAK3, ARHGEF9, GRIA3, SYP, PHF6, FGD1, ATRX, OFD1 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Early-Onset Epileptic Encephalopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RBFOX3, KPNA7, ARHGEF15, HCN2, TNK2, SLC12A5, ACY1, KCNH5, MTOR, NEDD4L, CLCN4, ZEB2, ATP6AP2, SYN1, ARHGEF9, IQSEC2, CNTNAP2, TCF4, KCNJ10, PNKP , (...)

View the complete list with 113 more genes
Specificity
1 %
Genes
100 %
Comprehensive Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RANGAP1, EFHC2, CELSR1, NIPA2, UBR5, VDAC1, BRD2, RBFOX3, KPNA7, CNTN2, ARHGEF15, PIK3AP1, FASN, RYR3, GABBR2, HCN2, TNK2, SRGAP2, GPHN, SLC12A5 , (...)

View the complete list with 427 more genes
Specificity
1 %
Genes
100 %
Rett Syndrome Mutation Analysis.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome Rearrangement (Deletion or Duplication).

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

MECP2
Specificity
100 %
Genes
100 %
X-chromosome High Resolution microarray analysis.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

SERPINA7, SAT1, SLC6A14, TBX22, COX7B, CHRDL1, VMA21, TRAPPC2, AMELX, CFP, POLA1, STS, ATP2B3, CLCN5, IGSF1, ZNF674, MAMLD1, ARSE, CCNQ, EDA , (...)

View the complete list with 140 more genes
Specificity
1 %
Genes
100 %
X-linked Intellectual Disability Panel.

By Blueprint Genetics in Finland.

ELK1, NXF5, DDX3X, ZNF674, PGK1, CLCN4, ZCCHC12, KLF8, IL1RAPL1, ZNF81, ARHGEF6, NSDHL, SOX3, SLC16A2, TAF1, BRWD3, ZDHHC9, RPL10, RBM10, SHROOM4 , (...)

View the complete list with 79 more genes
Specificity
2 %
Genes
100 %
Autism Spectrum Disorders Panel.

By Blueprint Genetics in Finland.

CNOT3, EN2, COL4A3BP, TCF20, KMT5B, CNTN6, CTNND2, TRIP12, BCL11A, POGZ, CC2D1A, RPL10, NLGN3, NLGN4X, CACNA1C, FOXP1, ADNP, PTCHD1, SHANK3, NSD1 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
100 %
Central Hypoventilation and Apnea Panel.

By Blueprint Genetics in Finland.

SLC6A5, GLRA1, EDN3, ZEB2, CHRNB1, CHRND, CHRNA1, COLQ, SCN4A, RAPSN, CHRNE, PHOX2B, CHAT, MECP2, RET
Specificity
7 %
Genes
100 %
Comprehensive Pulmonology Panel.

By Blueprint Genetics in Finland.

SLC34A2, PIH1D3, SLC6A5, GLRA1, ITGA3, SFTPA1, SFTPA2, DNAI1, SFTPB, DNAH5, NME8, SFTPC, ABCA3, NKX2-1, DNAH11, DNAI2, DNAAF2, RSPH4A, RSPH9, LTBP4 , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
100 %
Epileptic Encephalopathy Panel.

By Blueprint Genetics in Finland.

TBCK, RMND1, MRPL44, GTPBP3, HECW2, LYRM7, NACC1, UNC80, FAR1, GPHN, SLC12A5, APOPT1, FGF12, ECHS1, UBA5, TBCD, SERAC1, TBCE, SLC25A1, ASNS , (...)

View the complete list with 108 more genes
Specificity
1 %
Genes
100 %
Comprehensive Epilepsy Panel.

By Blueprint Genetics in Finland.

SNORD118, SLC39A8, YY1, TBCK, RMND1, MRPL44, GTPBP3, HECW2, WDR26, LYRM7, DARS, KCNH1, NACC1, DPYS, UNC80, FAR1, AIMP1, ECM1, GPHN, PIGT , (...)

View the complete list with 263 more genes
Specificity
1 %
Genes
100 %
Rett syndrome.

By Bioarray in Spain.

MECP2
Specificity
100 %
Genes
100 %
Angelman syndrome.

By Bioarray in Spain.

MECP2
Specificity
100 %
Genes
100 %
MeCP2 mutation detection.

By Tulane Hayward Genetics Center Molecular Diagnostics Lab Tulane University in United States.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

MECP2
Specificity
100 %
Genes
100 %
Rett syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CDKL5, MECP2
Specificity
50 %
Genes
100 %
Rett Plus Atypical Rett Syndrome Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

MEF2C, FOXG1, CDKL5, MECP2
Specificity
25 %
Genes
100 %
Exome.

By DNA CONSULT GENETICA E BIOTECNOLOGIA LTDA. in Brazil.

IPW, SMNDC1, GEMIN2, HERC2, ATXN8, CYP2C9, IL1RN, CCDC88C, VKORC1, CYP2D6, CYP2C19, F8, F9, MAGEL2, SOX9, RPL10, PTCHD1, SEMA3E, SHANK2, KCND3 , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
100 %
Rapid microarray (CGH and SNP).

By Allele Diagnostics Allele Diagnostics in United States.

CRK, SEM1, IGF2, FBXW4, YWHAE, TBX3, HDAC4, TRPS1, STS, GRIK2, FLI1, PREPL, MAMLD1, ARSE, IRF6, CCNQ, MNX1, NFIA, EDA, XK , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
100 %
High-Resolution Rapid Microarray (CGH and SNP).

By Allele Diagnostics Allele Diagnostics in United States.

CRK, SEM1, IGF2, FBXW4, YWHAE, TBX3, HDAC4, TRPS1, STS, GRIK2, FLI1, PREPL, MAMLD1, ARSE, IRF6, CCNQ, MNX1, NFIA, EDA, XK , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
100 %
INTELLECTUAL DEFICIT (X-LINKED).

By Laboratorio de Genetica Clinica SL in Spain.

RPS6KA3, ARX, MECP2
Specificity
34 %
Genes
100 %
RETT SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

FOXG1, CDKL5, MECP2
Specificity
34 %
Genes
100 %
Rett Syndrome, Sequencing MECP2 Gene.

By Reference Laboratory Genetics in Spain.

MECP2
Specificity
100 %
Genes
100 %
X-Linked Mental Retardation Type Lubs , Duplication MECP2 Gene.

By Reference Laboratory Genetics in Spain.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome, Deletions-Duplications (MLPA) MECP2 Gene.

By Reference Laboratory Genetics in Spain.

MECP2
Specificity
100 %
Genes
100 %
Rett Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 18 Genes.

By Reference Laboratory Genetics in Spain.

HERC2, BDNF, FOXP1, FOXP2, NTNG1, SHANK3, TCF4, KCNQ2, SCN2A, PLP1, MEF2C, FOXG1, CDKL5, ARX, ALDH5A1, STXBP1, MECP2, UBE3A
Specificity
6 %
Genes
100 %
Mental Retardation (Complete Panel) , Panel Massive Sequencing (NGS) 91 Genes.

By Reference Laboratory Genetics in Spain.

ZBTB18, HERC2, PPP2R1A, MYT1L, TRIO, POGZ, GNB1, CA8, CC2D1A, CRBN, GRIK2, MAN1B1, PRSS12, TRAPPC9, ZC3H14, CDH15, SOBP, LINS1, MED23, TECR , (...)

View the complete list with 71 more genes
Specificity
2 %
Genes
100 %
Autism Spectrum Disorders (Expanded Panel) , Panel Massive Sequencing (NGS) 77 Genes.

By Reference Laboratory Genetics in Spain.

BDNF, SLC6A4, AUTS2, KLHL3, PDE10A, SATB2, SOX5, DPP6, SLC9A9, SNRPN, RPL10, NLGN3, NLGN4X, HOXA1, CHD8, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
100 %
X-Linked Nonsyndromic Mental Retardation , Panel Massive Sequencing (NGS) 31 Genes.

By Reference Laboratory Genetics in Spain.

ZNF674, IL1RAPL1, ZNF81, ARHGEF6, BRWD3, SHROOM4, RPS6KA3, FTSJ1, GDI1, UPF3B, TSPAN7, DLG3, ZNF41, ZNF711, AFF2, AGTR2, HUWE1, NLGN4X, AP1S2, CASK , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
Rett syndrome.

By Labor Dr. Wisplinghoff in Germany.

MECP2
Specificity
100 %
Genes
100 %
MECP2 Duplication Syndrome: gene deletion/duplication.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MECP2
Specificity
100 %
Genes
100 %

Alternate names

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Is also known as ;severe congenital encephalopathy due to mecp2 mutation.



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK15 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14 GLYCOGEN STORAGE DISEASE XI; GSD11 ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13

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