NIPBL gene related symptoms and diseases
All the information presented here about the NIPBL gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NIPBL gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Very Common - Between 80% and 100% cases |
Sleep disturbance | Very Common - Between 80% and 100% cases |
Low posterior hairline | Very Common - Between 80% and 100% cases |
Micrognathia | Very Common - Between 80% and 100% cases |
Strabismus | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NIPBL gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Brachycephaly
- High palate
- Seizures
- Clinodactyly of the 5th finger
- Conductive hearing impairment
- Curly eyelashes
- Gastroesophageal reflux
- Autism
And 234 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NIPBL gene
Here you will find a list of rare diseases related to the NIPBL. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
5P13 MICRODUPLICATION SYNDROME
Alternate names
5P13 MICRODUPLICATION SYNDROME Is also known as dup(5)(p13), trisomy 5p13
Description
5p13 microduplication syndrome is a rare partial autosomal trisomy/tetrasomy characterized by global developmental delay, intellectual disability, autistic behavior, muscular hypotonia, macrocephaly and facial dysmorphism (frontal bossing, short palpebral fissures, low set, dysplastic ears, short or shallow philtrum, high arched or narrow palate, micrognathia). Other associated clinical features include sleep disturbances, seizures, aplasia/hypoplasia of the corpus callosum, skeletal abnormalities (large hands and feet, long fingers and toes, talipes).
Most common symptoms of 5P13 MICRODUPLICATION SYNDROME
- Intellectual disability
- Seizures
- Global developmental delay
- Generalized hypotonia
- Scoliosis
More info about 5P13 MICRODUPLICATION SYNDROME
CORNELIA DE LANGE SYNDROME
Alternate names
CORNELIA DE LANGE SYNDROME Is also known as brachmann-de lange syndrome
Description
Cornelia de Lange syndrome (CdLS) is a multisystem disorder with variable expression marked by a characteristic facial dysmorphism, variable degrees of intellectual deficit, severe growth retardation beginning before birth (2nd trimester), abnormal hands and feet (oligodactyly, or sometimes an even more severe amputation, and constant brachymetacarpia of the first metacarpus), and various other malformations (heart, kidney etc.).
Most common symptoms of CORNELIA DE LANGE SYNDROME
- Intellectual disability
- Seizures
- Short stature
- Microcephaly
- Nystagmus
More info about CORNELIA DE LANGE SYNDROME
SOURCES: ORPHANET
CORNELIA DE LANGE SYNDROME 1; CDLS1
Alternate names
CORNELIA DE LANGE SYNDROME 1; CDLS1 Is also known as typus degenerativus amstelodamensis, brachmann-de lange syndrome, cdl, de lange syndrome, cdls, bdls
Description
The Cornelia de Lange syndrome (CDLS) is a multisystem malformation syndrome recognized primarily on the basis of characteristic facial dysmorphism, including low anterior hairline, arched eyebrows, synophrys, anteverted nares, maxillary prognathism, long philtrum, thin lips, and 'carp' mouth, in association with prenatal and postnatal growth retardation, mental retardation and, in many cases, upper limb anomalies. However, there is wide clinical variability in this disorder, with milder phenotypes that may be difficult to ascertain on the basis of physical features (summary by Rohatgi et al., 2010).Boyle et al. (2015) provided a detailed review of CDLS, including clinical features, diagnosis, and genetic counseling.
Most common symptoms of CORNELIA DE LANGE SYNDROME 1; CDLS1
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Generalized hypotonia
More info about CORNELIA DE LANGE SYNDROME 1; CDLS1
SOURCES: OMIM
Search interest in NIPBL
Potential gene panels for NIPBL gene
PreSeek Non-invasive Prenatal Gene Sequencing Screen Panel
By Baylor Miraca Genetics Laboratories PreSeek Non-invasive Prenatal Gene Sequencing Screen that also includes the following genes: RIT1 BRAF SMC1A SOS1 SOS2 CDKL5 SYNGAP1 TSC1 TSC2 HDAC8
More info about this panelEpilepsy Advanced Sequencing and CNV Evaluation Panel
By Athena Diagnostics Inc Epilepsy Advanced Sequencing and CNV Evaluation that also includes the following genes: SCN1A SCN1B SCN2A SCN3A SCN5A SCN8A SCN9A SHH ST3GAL3 ST3GAL5
More info about this panelEpilepsy Advanced Sequencing and CNV Evaluation - Syndromic Disorders Panel
By Athena Diagnostics Inc Epilepsy Advanced Sequencing and CNV Evaluation - Syndromic Disorders that also includes the following genes: SYNGAP1 TBX1 TSC1 TSC2 SETBP1 PANK2 ADGRV1 ATP6V0A2 MAGI2 VPS13A
More info about this panelSyndromic Autism Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Syndromic Autism Panel that also includes the following genes: SCN1A SCN2A BRAF SLC2A1 SLC9A6 SMC1A KDM5C CDKL5 STXBP1 TBR1
More info about this panelCornelia de Lange syndrome Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Cornelia de Lange Syndrome Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCoffin-Siris Syndrome Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Coffin-Siris Syndrome Panel that also includes the following genes: SMARCA2 SMARCA4 SMARCB1 SMARCE1 ARID1A SMC1A SOX11 BTD HDAC8 ADNP
More info about this panelComprehensive Brain Malformation Panel Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Comprehensive Brain Malformation Panel that also includes the following genes: SHH STIL SIX3 SLC9A6 SOX2 CDKL5 TGIF1 MED12 CEP41 TUBA8
More info about this panelMicrocephaly Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Microcephaly that also includes the following genes: STIL SLC9A6 CDKL5 TCF4 UBE3A RAB18 SLC25A19 ZEB2 CASK PCNT
More info about this panelCornelia de Lange Syndrome NGS panel Panel
By Medical Genetics Laboratory, Kennedy Center Juliane Marie Center, Rigshospitalet Cornelia de Lange Syndrome NGS panel that also includes the following genes: HDAC8 SMC3 NIPBL RAD21
More info about this panelNIPBL sequencing Panel
By Genetic Services Laboratory University of Chicago
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome PLUS Sequencing Panel Panel
By Genetic Services Laboratory University of Chicago Cornelia de Lange Syndrome PLUS Sequencing Panel that also includes the following genes: ROR2 SMARCA2 SMARCA4 SMARCB1 SMARCE1 ARID1A SMC1A SOX11 WNT5A HDAC8
More info about this panelCornelia de Lange Syndrome Panel Panel
By Genetic Services Laboratory University of Chicago Cornelia de Lange Syndrome Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelNIPBL deletion/duplication analysis Panel
By Genetic Services Laboratory University of Chicago
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange PLUS Deletion/Duplication Panel Panel
By Genetic Services Laboratory University of Chicago Cornelia de Lange PLUS Deletion/Duplication Panel that also includes the following genes: ROR2 SMARCA2 SMARCA4 SMARCB1 SMARCE1 ARID1A SMC1A SOX11 WNT5A HDAC8
More info about this panelNIPBL Select Exons Sequencing Panel
By GeneDx
This panel specifically test the NIPBL gene.
More info about this panelNIPBL Remaining Exons Sequencing Panel
By GeneDx
This panel specifically test the NIPBL gene.
More info about this panelAutism/Intellectual Disability/Multiple Anomalies Panel
By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center Autism/Intellectual Disability/Multiple Anomalies that also includes the following genes: BDNF RPS6KA3 SCN1A BRAF SLC2A1 SLC6A4 SLC9A6 SMC1A KDM5C SOS1
More info about this panelAutismNext Panel
By Ambry Genetics AutismNext that also includes the following genes: SCN2A SLC6A8 SLC9A6 SMC1A CDKL5 SYNGAP1 TBR1 TCF4 MED12 TSC1
More info about this panelCdLSNext Panel
By Ambry Genetics CdLSNext that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCustomNext: Neuro Panel
By Ambry Genetics CustomNext: Neuro that also includes the following genes: RPL10 RPS6KA3 SCN1A SCN1B SCN2A SCN8A ST3GAL3 SLC16A2 SLC2A1 SLC35A2
More info about this panelNeurodevelopment-Expanded Panel
By Ambry Genetics Neurodevelopment-Expanded that also includes the following genes: RPL10 RPS6KA3 SCN1A SCN1B SCN2A SCN8A ST3GAL3 SLC16A2 SLC2A1 SLC35A2
More info about this panelIDNext Panel
By Ambry Genetics IDNext that also includes the following genes: RPL10 RPS6KA3 SCN2A SCN8A ST3GAL3 SLC16A2 SLC2A1 SLC6A8 SLC9A6 SMARCA2
More info about this panelNIPBL mutation analysis Panel
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam
This panel specifically test the NIPBL gene.
More info about this panelNIPBL. Complete sequencing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the NIPBL gene.
More info about this panelNIPBL, SMC1A, SMC3. NextGeneDx.Complete sequencing by NGS Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica NIPBL, SMC1A, SMC3. NextGeneDx.Complete sequencing by NGS that also includes the following genes: SMC1A SMC3 NIPBL
More info about this panelNIPBL. MLPA testing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the NIPBL gene.
More info about this panelNIPBL-Related Cornelia de Lange Syndrom Panel
By Unity of Clinical Genetics and Functional Genomics University of Zaragoza. Faculty of Medicine.
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Seq Analysis Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Cornelia de Lange Seq Analysis that also includes the following genes: SMC1A HDAC8 ASXL1 ANKRD11 SMC3 NIPBL ASXL3 RAD21
More info about this panelCornelia de Lange Seq + Del/Dup Panel Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Cornelia de Lange Seq + Del/Dup Panel that also includes the following genes: SMC1A HDAC8 ASXL1 ANKRD11 SMC3 NIPBL ASXL3 RAD21
More info about this panelCornelia de Lange Del/Dup Panel Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Cornelia de Lange Del/Dup Panel that also includes the following genes: SMC1A HDAC8 ASXL1 ANKRD11 SMC3 NIPBL ASXL3 RAD21
More info about this panelCornelia de Lange Syndrome (deletion/duplication analysis of NIPBL gene) Panel
By CGC Genetics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome (sequence analysis of NIPBL gene) Panel
By CGC Genetics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange syndrome (NGS panel for 5 genes) Panel
By CGC Genetics Cornelia de Lange syndrome (NGS panel for 5 genes) that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange Syndrome Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Cornelia de Lange Syndrome Sequencing Panel with CNV Detection that also includes the following genes: SMC1A HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelFacial Dysostosis Related Disorders Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Facial Dysostosis Related Disorders Sequencing Panel with CNV Detection that also includes the following genes: SF3B4 SMC1A TCF12 TCOF1 TWIST1 HDAC8 SRCAP POLR1C POLR1D CREBBP
More info about this panelCongenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Sequencing Panel with CNV Detection that also includes the following genes: ROBO2 SALL1 BMP4 BMP7 SIX1 SIX2 SIX5 SOX11 TBX18 HNF1B
More info about this panelCongenital Limb Malformation Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Congenital Limb Malformation Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP2 BMPR1B SF3B4 FBXW4 SHH BRCA2 SOX9 TBX15
More info about this panelCornelia de Lange Syndrome via NIPBL Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Cornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Sequencing Panel with CNV Detection that also includes the following genes: SMARCA4 SMARCB1 SMARCE1 ARID1A SMC1A SOX11 TAF1 TAF6 MED12 HDAC8
More info about this panelSkeletal Disorders and Joint Problems Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection that also includes the following genes: RMRP ROR2 RUNX2 SALL1 BMP1 BMP2 BMPR1B SF3B4 SH3BP2 FBXW4
More info about this panelCornelia de Lange syndrome Comprehensive panel Panel
By Connective Tissue Gene Tests Cornelia de Lange syndrome Comprehensive panel that also includes the following genes: SMC1A HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange syndrome Deletion / Duplication panel Panel
By Connective Tissue Gene Tests Cornelia de Lange syndrome Deletion / Duplication panel that also includes the following genes: SMC1A HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange syndrome NGS panel Panel
By Connective Tissue Gene Tests Cornelia de Lange syndrome NGS panel that also includes the following genes: SMC1A HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelMental retardation - different panels Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Mental retardation - different panels that also includes the following genes: RGS7 RIT1 RMRP BCS1L RPL10 RPS6KA3 RRAS SALL1 SC5D ATXN10
More info about this panelCornelia-de-Lange syndrome Panel
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the NIPBL gene.
More info about this panelCohesinopathies (Cornelia de Lange Syndrome) Panel
By MGZ Medical Genetics Center Cohesinopathies (Cornelia de Lange Syndrome) that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelMental Retardation and Dysmorphology - panels Panel
By MGZ Medical Genetics Center Mental Retardation and Dysmorphology - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panelSyndromal Diseases - panels Panel
By MGZ Medical Genetics Center Syndromal Diseases - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panelBrain Malformations / Neuronal Migration Disorders Panel
By MGZ Medical Genetics Center Brain Malformations / Neuronal Migration Disorders that also includes the following genes: RPL10 RPS6KA3 SCN1A SCN1B SCN2A SCN8A SGCE SGSH STIL SLC16A2
More info about this panelNIPBL-Related Cornelia de Lange Syndrome Panel
By Bioscientia GmbH Center for Human Genetics
This panel specifically test the NIPBL gene.
More info about this panelAllNeuro panel Panel
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panelCentoICU platinum plus Panel
By Centogene AG - the Rare Disease Company CentoICU platinum plus that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panelNew Born testing (CentoICU) Panel
By Centogene AG - the Rare Disease Company New Born testing (CentoICU) that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panelCornelia de Lange syndrome type 1 Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the NIPBL gene.
More info about this panelSingle gene testing NIPBL Panel
By CeGaT GmbH
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome Panel
By Asper Biogene Asper Biogene LLC Cornelia de Lange Syndrome that also includes the following genes: SMC1A TAF6 HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelAutism Spectrum Disorders Panel
By Asper Biogene Asper Biogene LLC Autism Spectrum Disorders that also includes the following genes: RPL10 SCN1A SCN2A BRAF SLC6A4 SLC6A8 CDKL5 MED12 TSC1 TSC2
More info about this panelCornelia-de-Lange syndrome 1 Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the NIPBL gene.
More info about this panelqChip Panel
By Quantitative Genomic Medicine Laboratories, SL qChip that also includes the following genes: RS1 RUNX2 SALL1 SCN1A BMPR1A SH2D1A SEM1 SHH SHOX SIM1
More info about this panelqGenEx Craniofacial Anomalies Panel
By Quantitative Genomic Medicine Laboratories, SL qGenEx Craniofacial Anomalies that also includes the following genes: RUNX2 SALL1 TSHZ1 BMP4 SEMA3E SF3B4 SH3BP2 SHH SIX1 SIX3
More info about this panelCornelia-de-Lange syndrome 1 Panel
By MedGene
This panel specifically test the NIPBL gene.
More info about this panelInvitae Cornelia de Lange Syndrome Panel Panel
By Invitae Invitae Cornelia de Lange Syndrome Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange syndrome: NIPBL gene sequence analysis Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange syndrome: NIPBL gene deletions-duplications analysis (MLPA) Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange syndrome Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Cornelia de Lange syndrome that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange Syndrome: NIPBL Gene Deletion/Duplication Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome: NIPBL Gene Sequencing Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics
This panel specifically test the NIPBL gene.
More info about this panelProportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Proportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel that also includes the following genes: ROR2 RPS6KA3 BLM SHOX SHOX2 SMARCAL1 SMC1A SOS1 SOX2 SOX3
More info about this panelAutism Spectrum Disorders: Tier 2 Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Autism Spectrum Disorders: Tier 2 Panel that also includes the following genes: SCN1A BRAF SLC2A1 SLC9A6 SMARCB1 SMC1A KDM5C CDKL5 TCF4 MED12
More info about this panelLimb Malformation: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Limb Malformation: Sequencing Panel that also includes the following genes: ROR2 SALL1 BMP2 BMPR1B FBXW4 SHH SOX9 TBX15 TBX3 TBX5
More info about this panelSkeletal Dysplasia: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Skeletal Dysplasia: Sequencing Panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SHOX SLC25A12 SLC26A2
More info about this panelCornelia de Lange Syndrome: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Cornelia de Lange Syndrome: Sequencing Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelAutism Spectrum Disorders: Tier 2 Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Autism Spectrum Disorders: Tier 2 Deletion/Duplication Panel that also includes the following genes: SCN1A BRAF SLC2A1 SLC9A6 SMARCB1 SMC1A KDM5C CDKL5 TCF4 MED12
More info about this panelCornelia de Lange Syndrome: Deletion/Duplication Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Cornelia de Lange Syndrome: Deletion/Duplication Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelAutism NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Autism NGS Panel that also includes the following genes: RPL10 BDNF SCN1A SCN2A BRAF SLC6A4 SLC9A6 SMC1A KDM5C SNRPN
More info about this panelEpilepsy NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Epilepsy NGS Panel that also includes the following genes: BCS1L SCN10A SCN1A SCN1B SCN2A SCN2B SCN3A SCN4A SCN4B SCN5A
More info about this panelIntellectual Disability NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Intellectual Disability NGS Panel that also includes the following genes: BCS1L RPS6KA3 SACS BIN1 SCN1A SCN8A SDCCAG8 SGCA SGSH ST3GAL3
More info about this panelShort Stature NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Short Stature NGS Panel that also includes the following genes: SMC1A SOS1 CREBBP DHCR7 NIPBL EP300 FGD1 KRAS PTPN11 RAF1
More info about this panelCornelia De Lange Syndrome NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Cornelia De Lange Syndrome NGS Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelSkeletal Dysplasias NGS panel Panel
By Fulgent Genetics Fulgent Genetics Skeletal Dysplasias NGS panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SLC25A12 SLC26A2 SMARCAL1
More info about this panelNIPBL Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NIPBL gene.
More info about this panelComprehensive Epilepsy NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Comprehensive Epilepsy NGS Panel that also includes the following genes: BCS1L RYR3 SCN10A SCN1A SCN1B SCN2A SCN2B SCN3A SCN4A SCN4B
More info about this panelComprehensive Short Stature Syndrome Panel Panel
By Blueprint Genetics Comprehensive Short Stature Syndrome Panel that also includes the following genes: RIT1 BCS1L RRAS SHOX BRAF SMC1A SOS1 SOX2 SOX3 STAT5B
More info about this panelFacial Dysostosis and Related Disorders Panel Panel
By Blueprint Genetics Facial Dysostosis and Related Disorders Panel that also includes the following genes: SF3B4 SMC1A TCOF1 TWIST1 UBE2A HDAC8 SRCAP EVC2 POLR1C POLR1D
More info about this panelComprehensive Skeletal Dysplasias and Disorders Panel Panel
By Blueprint Genetics Comprehensive Skeletal Dysplasias and Disorders Panel that also includes the following genes: RMRP ROR2 BGN RUNX2 BMP1 BMP2 BMPR1B SF3B4 SH3BP2 SHOX
More info about this panelCornelia de Lange Syndrome Panel Panel
By Blueprint Genetics Cornelia de Lange Syndrome Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelLimb Malformations Panel Panel
By Blueprint Genetics Limb Malformations Panel that also includes the following genes: SALL1 SF3B4 BRCA2 SMC1A TBX3 TBX5 WNT7A XRCC2 HDAC8 NSDHL
More info about this panelComprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Panel
By Blueprint Genetics Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel that also includes the following genes: RIT1 RMRP BCS1L ROR2 BGN RRAS RUNX2 BMP1 BMP2 SEC24D
More info about this panelCornelia de Lange syndrome type 1 Panel
By Bioarray
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange syndrome Panel
By Bioarray
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange NGS and Deletion/Duplication Panel Panel
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children Cornelia de Lange NGS and Deletion/Duplication Panel that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelNIPBL Gene Sequencing and Deletion/Duplication Analysis Panel
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
This panel specifically test the NIPBL gene.
More info about this panelRapid microarray (CGH and SNP) Panel
By Allele Diagnostics Allele Diagnostics Rapid microarray (CGH and SNP) that also includes the following genes: RPS19 RUNX2 SALL1 SCN1A SCN2A SDHB SDHD BMPR1A SGCE SH2D1A
More info about this panelHigh-Resolution Rapid Microarray (CGH and SNP) Panel
By Allele Diagnostics Allele Diagnostics High-Resolution Rapid Microarray (CGH and SNP) that also includes the following genes: RPS19 RUNX2 SALL1 SCN1A SCN2A SDHB SDHD BMPR1A SGCE SH2D1A
More info about this panelCORNELIA DE LANGE SYNDROME (AUTOSOMAL DOMINANT) Panel
By Laboratorio de Genetica Clinica SL CORNELIA DE LANGE SYNDROME (AUTOSOMAL DOMINANT) that also includes the following genes: SMC3 NIPBL
More info about this panelCORNELIA DE LANGE SYNDROME: NGS PANEL Panel
By Laboratorio de Genetica Clinica SL CORNELIA DE LANGE SYNDROME: NGS PANEL that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelCornelia de Lange Syndrome Type 1 , Sequencing NIPBL Gene Panel
By Reference Laboratory Genetics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome Type 1 , Deletions-Duplications (MLPA) NIPBL Gene Panel
By Reference Laboratory Genetics
This panel specifically test the NIPBL gene.
More info about this panelCornelia de Lange Syndrome , Panel massive Sequencing (NGS) 5 Genes Panel
By Reference Laboratory Genetics Cornelia de Lange Syndrome , Panel massive Sequencing (NGS) 5 Genes that also includes the following genes: SMC1A HDAC8 SMC3 NIPBL RAD21
More info about this panelAutism Spectrum Disorders (Expanded Panel) , Panel Massive Sequencing (NGS) 77 Genes Panel
By Reference Laboratory Genetics Autism Spectrum Disorders (Expanded Panel) , Panel Massive Sequencing (NGS) 77 Genes that also includes the following genes: RPL10 BDNF SCN1A SCN2A BRAF SLC6A4 SLC9A6 SMC1A KDM5C SNRPN
More info about this panelTempus xO assay Panel
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
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