Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 1; Mpph1

Description

This disorder comprises megalencephaly, hydrocephalus, and polymicrogyria; polydactyly may also be seen. There is considerable phenotypic similarity between this disorder and the megalencephaly-capillary malformation syndrome (MCAP ) (summary by Gripp et al., 2009). Genetic Heterogeneity the Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus SyndromeSee also MPPH2 (OMIM ), caused by mutation in the AKT3 gene (OMIM ) on chromosome 1q43-q44; and MPPH3 (OMIM ), caused by mutation in the CCND2 gene (OMIM ) on chromosome 12p13.

Clinical Features

Top most frequent phenotypes and symptoms related to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 1; Mpph1

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Pica
  • Hypertelorism
  • Motor delay
  • Ptosis
  • Abnormal facial shape
  • Depressed nasal bridge
And another 39 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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Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 1; Mpph1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Polymicrogyria Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

TUBB3, TUBA1A, WDR62, NDE1, RAB3GAP1, TUBA8, ADGRG1, TUBB2B, KIF1BP, GPSM2, RAB3GAP2, RAB18, OCLN, CCND2, AKT3-IT1, TBC1D20, RTTN
Specificity
6 %
Genes
34 %
Cerebral Cortical Malformation Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1 , (...)

View the complete list with 34 more genes
Specificity
4 %
Genes
67 %
Polymicrogyria Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

TUBB3, TUBA1A, WDR62, NDE1, RAB3GAP1, TUBA8, ADGRG1, TUBB2B, KIF1BP, GPSM2, RAB3GAP2, RAB18, OCLN, CCND2, AKT3-IT1, TBC1D20, RTTN
Specificity
6 %
Genes
34 %
Cerebral Cortical Malformations Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

TUBB3, ATP6V0A2, SRD5A3, TUBA1A, ARX, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, B4GAT1, POMGNT2, LARGE1, B3GALNT2, ARFGEF2, DCX, NDE1 , (...)

View the complete list with 34 more genes
Specificity
4 %
Genes
67 %
Megalencephaly-polymicrogyria and dysplastic megalencephaly (NGS panel of 8 genes).

By CGC Genetics in Portugal.

DEPDC5, MTOR, EZH2, PIK3CA, PIK3R2, AKT3, CCND2, NPRL3
Specificity
38 %
Genes
100 %
Megalencephaly-polymicrogyria and dysplastic megalencephaly (NGS panel of 8 genes).

By CGC Genetics in Portugal.

DEPDC5, MTOR, EZH2, PIK3CA, PIK3R2, AKT3, CCND2, NPRL3
Specificity
38 %
Genes
100 %
Hydrocephalus Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

PTEN, L1CAM, POMT1, AP1S2, FLVCR2, DNAI1, P4HB, ZIC3, PIK3R2, AKT3, CCND2, CRB2, CCDC88C, MPDZ, WDR81, EML1, HDAC6
Specificity
18 %
Genes
100 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Comprehensive test.

By Connective Tissue Gene Tests in United States.

PIK3R2, AKT3, CCND2
Specificity
100 %
Genes
100 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus NGS test.

By Connective Tissue Gene Tests in United States.

PIK3R2, AKT3, CCND2
Specificity
100 %
Genes
100 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Deletion / Duplication test.

By Connective Tissue Gene Tests in United States.

PIK3R2, AKT3, CCND2
Specificity
100 %
Genes
100 %
Macrocephaly.

By MGZ Medical Genetics Center in Germany.

PTEN, ASPA, TSC2, TSC1, NSD1, PTCH1, CDKN1C, GPC3, MLC1, EIF2B5, L1CAM, WASHC5, SETD2, OFD1, GRIA3, SYN1, CUL4B, RAB39B, GFAP, MED12 , (...)

View the complete list with 22 more genes
Specificity
8 %
Genes
100 %
Mental Retardation and Dysmorphology - panels.

By MGZ Medical Genetics Center in Germany.

FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2 , (...)

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

By MGZ Medical Genetics Center in Germany.

FMR1, UBE3A, PTEN, RECQL4, AGL, ATP7A, GAA, LRP5, SLC37A4, GNPTAB, GLB1, HSD17B10, OCRL, JAG1, NDP, HPRT1, NHS, RAF1, SMPD1, MECP2 , (...)

View the complete list with 322 more genes
Specificity
1 %
Genes
100 %
Brain Malformations / Neuronal Migration Disorders.

By MGZ Medical Genetics Center in Germany.

FMR1, UBE3A, PTEN, APP, TUBB3, HSD17B10, HPRT1, PANK2, FH, MECP2, GAMT, STXBP1, TUBA1A, SLC25A22, GLDC, GK, MAOA, ACSL4, SLC9A6, ALDH7A1 , (...)

View the complete list with 246 more genes
Specificity
2 %
Genes
100 %
Megalencephaly.

By MGZ Medical Genetics Center in Germany.

PTEN, TSC2, TSC1, PIK3CA, PIK3R2, AKT3, AKT1, CCND2
Specificity
38 %
Genes
100 %
RASopathies Panel.

By CeGaT GmbH in Germany.

RAF1, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, CBL, NF1, RASA1, SPRED1, RASA2, RRAS, A2ML1, STAMBP, PIK3CA , (...)

View the complete list with 3 more genes
Specificity
14 %
Genes
100 %
RASopathies Panel.

By CeGaT GmbH in Germany.

RAF1, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, CBL, NF1, RASA1, SPRED1, RASA2, RRAS, A2ML1, STAMBP, PIK3CA , (...)

View the complete list with 3 more genes
Specificity
14 %
Genes
100 %
RASopathies Panel.

By CeGaT GmbH in Germany.

RAF1, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, CBL, NF1, RASA1, SPRED1, RASA2, RRAS, A2ML1, STAMBP, PIK3CA , (...)

View the complete list with 3 more genes
Specificity
14 %
Genes
100 %
Single gene testing CCND2.

By CeGaT GmbH in Germany.

CCND2
Specificity
100 %
Genes
34 %
Brain malformations.

By Asper Biogene Asper Biogene LLC in Estonia.

TUBB3, INPP5E, CC2D2A, ATP6V0A2, SRD5A3, TMEM67, NPHP1, CEP290, DLD, SLC25A19, MECP2, PDHB, TUBA1A, RARS2, PDP1, GCSH, GLDC, AMT, PDHA1, DLAT , (...)

View the complete list with 125 more genes
Specificity
3 %
Genes
100 %
CCND2.

By Fulgent Genetics Fulgent Genetics in United States.

CCND2
Specificity
100 %
Genes
34 %
Macrocephaly / Overgrowth Syndrome Panel.

By Blueprint Genetics in Finland.

PTEN, ASPA, TSC2, TSC1, NSD1, PTCH1, CDKN1C, GPC3, MLC1, EIF2B5, L1CAM, WASHC5, SETD2, PIGA, OFD1, GRIA3, SYN1, CUL4B, RAB39B, GFAP , (...)

View the complete list with 23 more genes
Specificity
7 %
Genes
100 %
FoundationOne® Heme.

By Foundation Medicine, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, PC, FOXL2, HNF1A, WT1, RB1, RET, TNFRSF11A, CPS1, SDHC , (...)

View the complete list with 385 more genes
Specificity
1 %
Genes
100 %
Guardant360.

By Guardant Health in United States.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, HNF1A, RB1, RET, RAF1, IDH2, FGFR3, AR, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11 , (...)

View the complete list with 53 more genes
Specificity
2 %
Genes
34 %
NeoTYPE® Discovery Profile for Solid Tumors.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, FOXL2, HNF1A, WT1, RB1, RET, SDHC, RAF1, FH , (...)

View the complete list with 295 more genes
Specificity
1 %
Genes
100 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, FOXL2, HNF1A, PPARG, COL1A1, WT1, RB1, SDHAF2 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
100 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3.

By Labor Dr. Wisplinghoff in Germany.

CCND2
Specificity
100 %
Genes
34 %
Tempus xT assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ATP7B, FOXL2, HNF1A, WT1, RB1 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
100 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
100 %
Megalencephaly-Postaxial Polydactyly-Polymicrogyria-Hydrocephalus Syndrome (MPPH Syndrome): gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

PIK3R2, AKT3, CCND2
Specificity
100 %
Genes
100 %
Somatic Overgrowth Gene Panel.

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine in United States.

MTOR, PIK3CA, AKT2, GNAQ, GNA11, PIK3R2, AKT3, AKT1
Specificity
25 %
Genes
67 %
Segmental Overgrowth Disorders - NGS panel (8 genes).

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

PTEN, TSC2, TSC1, MTOR, PIK3CA, PIK3R2, AKT3, AKT1
Specificity
25 %
Genes
67 %
PIK3R2. Complete sequencing.

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

PIK3R2
Specificity
100 %
Genes
34 %
Macrocephaly (NGS panel for 16 genes).

By CGC Genetics in Portugal.

PTEN, ASPA, NSD1, GPC3, MLC1, PIGA, PIGN, GFAP, MED12, NFIX, EZH2, PIK3CA, DHCR24, PIK3R2, AKT3, HEPACAM
Specificity
13 %
Genes
67 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH, sequence analysis of PIK3R2 gene).

By CGC Genetics in Portugal.

PIK3R2
Specificity
100 %
Genes
34 %
Mental retardation - different panels.

By Institute of Human Genetics Cologne University in Germany.

FMR1, UBE3A, PTEN, MCCC1, MCCC2, ACAD9, PC, ANKH, HLCS, ATP7A, AUH, B4GALT7, BCKDHA, BCKDHB, BCS1L, C12orf65, ADSL, MMACHC, PRKCG, PAX6 , (...)

View the complete list with 847 more genes
Specificity
1 %
Genes
67 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.

By Centogene AG - the Rare Disease Company in Germany.

PIK3R2
Specificity
100 %
Genes
34 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
67 %
Neuronal Migration Disorders Panel.

By CeGaT GmbH in Germany.

TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
34 %
Macrocephaly Panel.

By CeGaT GmbH in Germany.

PTEN, GCDH, ASPA, NSD1, GPC3, MLC1, PIGA, PIGN, GFAP, MED12, NFIX, EZH2, PIK3CA, DHCR24, PIK3R2, AKT3, HEPACAM
Specificity
12 %
Genes
67 %
Neuronal Migration Disorders Panel.

By CeGaT GmbH in Germany.

TUBB3, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, ISPD, LAMA2, B4GAT1, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
34 %
Macrocephaly Panel.

By CeGaT GmbH in Germany.

PTEN, GCDH, ASPA, NSD1, GPC3, MLC1, PIGA, PIGN, GFAP, MED12, NFIX, EZH2, PIK3CA, DHCR24, PIK3R2, AKT3, HEPACAM
Specificity
12 %
Genes
67 %
Single gene testing PIK3R2.

By CeGaT GmbH in Germany.

PIK3R2
Specificity
100 %
Genes
34 %
Invitae Overgrowth and Macrocephaly Syndromes Panel.

By Invitae in United States.

PTEN, NSD1, CDKN1C, GPC3, NF1, SETD2, PHF6, CUL4B, MED12, SPRED1, DNMT3A, NFIX, EZH2, GLI3, AKT2, PIK3R2, AKT3, KPTN, DIS3L2, NPR2
Specificity
10 %
Genes
67 %
NOONAN, LEOPARD, COSTELLO and CARDIOFACIOCUTANEOUS SYNDROME.

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

PRKCG, RAF1, IL2RG, FGFR3, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, CBL, MET, NF1, SHOX, ANKRD11, SPRED1 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
34 %
PIK3R2.

By Fulgent Genetics Fulgent Genetics in United States.

PIK3R2
Specificity
100 %
Genes
34 %
Neuronal Migration Disorder Panel.

By Blueprint Genetics in Finland.

TUBB3, ATP6V0A2, FH, TUBA1A, ARX, MEF2C, WDR62, FKTN, PHGDH, L1CAM, DYNC1H1, POMT1, ISPD, LAMA2, POMGNT2, RXYLT1, LARGE1, B3GALNT2, COL4A1, ARFGEF2 , (...)

View the complete list with 38 more genes
Specificity
4 %
Genes
67 %
Somatic Overgrowth Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

PTEN, IDH2, TSC2, TSC1, RASA1, MTOR, PIK3CA, AKT2, GNAQ, IDH1, GNA11, PIK3R2, AKT3, AKT1, SMO
Specificity
14 %
Genes
67 %
Solid Tumor Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, FOXL2, PPARG, WT1, RB1, RET, RAF1, IDH2, FGFR3, AR, BRAF, CREBBP, HRAS, KRAS , (...)

View the complete list with 102 more genes
Specificity
2 %
Genes
67 %
Gynecologic Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, FOXL2, RB1, BCOR, FGFR3, BRAF, HRAS, KRAS, MAP2K1, NRAS, FGFR2, MAP2K2, ATM, STK11 , (...)

View the complete list with 30 more genes
Specificity
4 %
Genes
67 %
Megalencephaly-Polymicrogyria-Postaxial Polydactyly-Hydrocephalus Type 1 , Sequencing PIK3R2 Gene.

By Reference Laboratory Genetics in Spain.

PIK3R2
Specificity
100 %
Genes
34 %
Polymicrogyria , Panel Massive Sequencing (NGS) 10 Genes.

By Reference Laboratory Genetics in Spain.

TUBB3, TUBA1A, FIG4, TUBA8, ADGRG1, SRPX2, TUBB2B, PIK3R2, AKT3, OCLN
Specificity
20 %
Genes
67 %
Macrocephaly , Panel Massive Sequencing (NGS) 16 Genes.

By Reference Laboratory Genetics in Spain.

PTEN, ASPA, NSD1, GPC3, MLC1, PIGA, PIGN, GFAP, MED12, NFIX, EZH2, PIK3CA, DHCR24, PIK3R2, AKT3, HEPACAM
Specificity
13 %
Genes
67 %
Malformations of Cortical Development , Panel Massive Sequencing (NGS) 38 Genes.

By Reference Laboratory Genetics in Spain.

TUBB3, TUBA1A, ARX, FOXG1, WDR62, FKTN, POMGNT1, FKRP, DYNC1H1, POMT2, POMT1, LAMA2, LARGE1, ASPM, COL4A1, ARFGEF2, DCX, NDE1, RELN, TUBA8 , (...)

View the complete list with 18 more genes
Specificity
6 %
Genes
67 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1.

By Labor Dr. Wisplinghoff in Germany.

PIK3R2
Specificity
100 %
Genes
34 %
152 Integrated Advantage NGS Solid Tumor Panel.

By Integrated Molecular Diagnostics Pathology, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, MLH1, PTEN, TP53, RB1, RET, RAF1, IDH2, TYMP, STAT3, FGFR3, AR, FANCC, BRAF, HRAS, KRAS , (...)

View the complete list with 132 more genes
Specificity
2 %
Genes
67 %
AKT3. Complete sequencing.

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

AKT3
Specificity
100 %
Genes
34 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH, sequence analysis of AKT3 gene).

By CGC Genetics in Portugal.

AKT3
Specificity
100 %
Genes
34 %
Microcephaly panel.

By Centogene AG - the Rare Disease Company in Germany.

SLC25A19, DNM1L, WDR62, POMT1, MCPH1, ASPM, CENPJ, NDE1, PAFAH1B1, STIL, TUBB2B, PNKP, CASK, CEP152, CDK5RAP2, PCNT, AP4M1, KIF11, EFTUD2, IER3IP1 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
34 %
Hemimegalencephaly.

By Centogene AG - the Rare Disease Company in Germany.

AKT3
Specificity
100 %
Genes
34 %
AKT3.

By Amplexa Genetics Amplexa Genetics A/S in Denmark.

AKT3
Specificity
100 %
Genes
34 %
Single gene testing AKT3.

By CeGaT GmbH in Germany.

AKT3
Specificity
100 %
Genes
34 %
Microcephaly NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SLC25A19, DNM1L, RARS2, WDR62, MRE11, VRK1, POMT1, MCPH1, CENPJ, NDE1, PQBP1, TSEN54, PAFAH1B1, STIL, TUBB2B, PNKP, CASK, TSEN34, TSEN2, CEP152 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
34 %
AKT3.

By Fulgent Genetics Fulgent Genetics in United States.

AKT3
Specificity
100 %
Genes
34 %
Comprehensive Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, AUH, BCS1L, TWNK, C12orf65, ADSL, PAX6, AMACR, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2 , (...)

View the complete list with 427 more genes
Specificity
1 %
Genes
34 %
Microcephaly and Pontocerebellar Hypoplasia Panel.

By Blueprint Genetics in Finland.

RARS2, GFM1, WDR62, MRE11, PHGDH, DYNC1H1, VRK1, POMT1, MCPH1, ASPM, MBD5, CENPJ, NDE1, PQBP1, TSEN54, PAFAH1B1, STIL, TUBB2B, KANSL1, DYRK1A , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
34 %
Polymicrogyria Panel.

By Blueprint Genetics in Finland.

TUBB3, FH, TUBA1A, WDR62, NDE1, TUBA8, ADGRG1, SRPX2, TUBB2B, KIF1BP, LAMC3, NSDHL, TUBB2A, GPSM2, RAB18, AKT3, OCLN
Specificity
6 %
Genes
34 %
Genitourinary Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, VHL, MLH1, PTEN, TP53, PPARG, FGFR3, AR, BRAF, CREBBP, HRAS, NRAS, FGFR2, TSC2, TSC1, ATM, PTCH1, CDKN2A, MET , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
34 %
Head & Neck Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, APC, PTEN, TP53, RB1, HRAS, KRAS, NRAS, NSD1, ATM, CDKN2A, SMAD4, NF1, KMT2D, MTOR, NOTCH1, TGFBR2, KDM6A, EP300 , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
34 %
Thoracic Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TP53, RB1, RET, BRAF, HRAS, KRAS, NRAS, RIT1, TSC2, TSC1, ALK, ATM, STK11, CDKN2A, MET, NTRK1, NF1, FGFR1, KMT2D, MED12 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
34 %
OmniSeq Comprehensive.

By OmniSeq, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, MLH1, PTEN, TP53, FOXL2, HNF1A, PPARG, WT1, RB1, RET, RAF1, IDH2, SOX2, STAT3, PNP, FGFR3 , (...)

View the complete list with 124 more genes
Specificity
1 %
Genes
34 %
Solid Tumor Targeted Mutation and Fusion Panel.

By Providence Regional Laboratories Providence Health and Services in United States.

PPARG, RET, RAF1, IDH2, FGFR3, AR, BRAF, HRAS, KRAS, MAP2K1, NRAS, FGFR2, MAP2K2, ALK, CDK4, MET, NTRK1, FGFR1, CTNNB1, MTOR , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
34 %
Megalencephaly-Polymicrogyria-Postaxial Polydactyly-Hydrocephalus Type 2 , Sequencing AKT3 Gene.

By Reference Laboratory Genetics in Spain.

AKT3
Specificity
100 %
Genes
34 %
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2.

By Labor Dr. Wisplinghoff in Germany.

AKT3
Specificity
100 %
Genes
34 %

Alternate names

Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 1; Mpph1 Is also known as megalencephaly, polymicrogyria, mega corpus callosum syndrome;mpph, meg-pmg-megacc syndrome, megalencephaly, mega corpus callosum, and complete lack of motor development;mpph syndrome.



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