CDH23 gene related symptoms and diseases

All the information presented here about the CDH23 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC,ORPHANET.

Top 5 symptoms associated to CDH23 gene



Symptoms // Phenotype % Cases
Headache 43%
Autosomal recessive inheritance 43%
Hemianopia 43%
Fatigue 43%
Osteoporosis 43%

Other less frequent symptoms

Patients with CDH23 gene alterations may also develop some of the following symptoms and phenotypes:

28% Growth hormone excess 28% Hypertension 28% Heteronymous hemianopia 28% Diplopia 28% Progressive visual loss 28% Cataract 28% Pallor 28% Cranial nerve paralysis

And 137 more phenotypes.
View the complete list

Rare diseases associated to CDH23 gene

Here you can will find a list of rare diseases related to the CDH23. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12

Most common symptoms of DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12

  • Prelingual sensorineural hearing impairment
  • Abnormality of the eye
  • Autosomal recessive inheritance


More info about DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12

SOURCES: OMIM

PITUITARY ADENOMA 5, MULTIPLE TYPES; PITA5

Description

Both familial and sporadic pituitary adenomas have been found to be caused by germline mutation in the CDH23 gene. Familial pituitary adenoma types include growth hormone (GH)-secreting and nonfunctional tumors. Sporadic pituitary adenoma types include GH-secreting, nonfunctional, prolactin (PRL)-secreting, adrenocorticotropin (ACTH)-secreting, thyroid-stimulating hormone (TSH)-secreting, and plurihormonal (GH and TSH) tumors.For a general description and a discussion of genetic heterogeneity of pituitary adenomas, see PITA1 (OMIM ).


More info about PITUITARY ADENOMA 5, MULTIPLE TYPES; PITA5

SOURCES: OMIM

USHER SYNDROME TYPE 1D

Description

Usher syndrome type I is an autosomal recessive condition characterized by profound congenital hearing impairment with unintelligible speech, early retinitis pigmentosa (usually evident within the first decade), and constant vestibular dysfunction. Type I is distinguished from type II (OMIM ) on the basis of severity of hearing loss and the extent of vestibular involvement. Type I patients are profoundly deaf, whereas type II patients are 'hard of hearing.' Vestibular function is defective in type I patients, whereas type II patients have normal vestibular function (Moller et al., 1989). Patients with type III (USH3 ) have progressive hearing loss.For a discussion of genetic heterogeneity of Usher syndrome type I, see {276900}.

Most common symptoms of USHER SYNDROME TYPE 1D

  • Vestibular dysfunction
  • Rod-cone dystrophy
  • Hearing impairment
  • Autosomal recessive inheritance


More info about USHER SYNDROME TYPE 1D

SOURCES: OMIM

PITUITARY ADENOMA 4, ACTH-SECRETING; PITA4

Alternate names

PITUITARY ADENOMA 4, ACTH-SECRETING; PITA4 Is also known as cushing disease, pituitary;

Description

Adrenocorticotropic hormone (ACTH) hypersecretion by corticotroph adenomas of the pituitary result in excess cortisol secretion, or Cushing disease. The clinical features of Cushing disease include central obesity, moon facies, 'buffalo hump,' diabetes, hypertension, fatigue, easy bruising, depression, and reproductive disorders. Cushing disease is associated with increased morbidity and mortality, mainly due to cardiovascular or cerebrovascular disease and infections (summary by Perez-Rivas et al., 2015).Mutations in the USP8 gene, leading to an upregulated epidermal growth factor receptor (EGFR ) pathway, have been identified in about 36 to 62% of corticotroph adenomas (summary by Mete and Lopes, 2017).

Most common symptoms of PITUITARY ADENOMA 4, ACTH-SECRETING; PITA4

  • Alkalosis
  • Abnormal fear/anxiety-related behavior
  • Psychotic mentation
  • Mood changes
  • Metrorrhagia


More info about PITUITARY ADENOMA 4, ACTH-SECRETING; PITA4

SOURCES: OMIM ORPHANET

PROLACTINOMA

Alternate names

PROLACTINOMA Is also known as prolactinoma, familial;

Description

Prolactin-secreting pituitary adenoma, or prolactinoma, is the most common type of hormonally active pituitary adenoma. These tumors can also be seen as a feature of multiple endocrine neoplasia type I (MEN1 ).See also {102200} for a discussion of familial isolated pituitary adenoma (FIPA) and acromegaly due to a growth hormone (GH )-secreting pituitary adenoma, which are also caused by mutation in the AIP gene.Schlechte (2003) discussed prolactinoma in general terms as a clinical, diagnostic, and therapeutic problem.

Most common symptoms of PROLACTINOMA

  • Prolactinoma
  • Heteronymous hemianopia
  • Abnormality of hair density
  • Internal ophthalmoplegia
  • Fourth cranial nerve palsy


More info about PROLACTINOMA

SOURCES: OMIM ORPHANET

TSH-SECRETING PITUITARY ADENOMA

Most common symptoms of TSH-SECRETING PITUITARY ADENOMA

  • Thyroid crisis
  • Heteronymous hemianopia
  • Abnormal visual field test
  • Abnormality of hair density
  • Euthyroid hyperthyroxinemia


More info about TSH-SECRETING PITUITARY ADENOMA

SOURCES: ORPHANET

USHER SYNDROME TYPE 1G

Alternate names

USHER SYNDROME TYPE 1G Is also known as ;

Description

Usher syndrome is an autosomal recessive disorder associated with sensorineural hearing impairment and progressive visual loss attributable to retinitis pigmentosa. The syndrome is both clinically and genetically heterogeneous. Of the 3 different clinical types that have been described, USH1 (OMIM ), consisting of the association of profound congenital deafness, constant vestibular dysfunction, and prepubertal onset retinitis pigmentosa, is the most severe.

Most common symptoms of USHER SYNDROME TYPE 1G

  • Hypoplasia of the nasal bone
  • Abnormality of cochlea
  • Vestibular hypofunction
  • Scotoma
  • Subcortical cerebral atrophy


More info about USHER SYNDROME TYPE 1G

SOURCES: ORPHANET OMIM

Potential gene panels for CDH23 gene

MitoMet®Plus aCGH Analysis Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States. MitoMet®Plus aCGH Analysis that also includes the following genes: BEST1 OPN1MW HNF1A HBB MUTYH NEUROD1 SPATA7 RAX BRCA1 FBLN5 And 627 more,

More info about this panel

CDH23 Sequence Analysis Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States.

This panel specifically test the CDH23 gene.

More info about this panel

CDH23 Sequence Analysis (Familial Mutation/Variant Analysis) Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States.

This panel specifically test the CDH23 gene.

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CDH23 Sequence Analysis (Prenatal Diagnosis) Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States.

This panel specifically test the CDH23 gene.

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GeneAware Complete Panel Version 2 (Female) Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States. GeneAware Complete Panel Version 2 (Female) that also includes the following genes: FMR1 PTS ADAMTS2 ALPL ADA ABCD1 BTD HSD17B4 ATM ATP7B And 149 more,

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GeneAware Complete Panel Version 2 (Male) Panel

By Baylor Miraca Genetics Laboratories Baylor College of Medicine in United States. GeneAware Complete Panel Version 2 (Male) that also includes the following genes: PTS ADAMTS2 ALPL ADA BTD HSD17B4 ATM ATP7B BCS1L BCKDHB And 139 more,

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NGS Hearing Loss Panel Panel

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States. NGS Hearing Loss Panel that also includes the following genes: EYA1 TMPRSS3 SIX1 CRYM CIB2 FOXI1 COL11A2 TECTA CLPP CACNA1D And 81 more,

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OtoSCOPE Panel

By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics in United States. OtoSCOPE that also includes the following genes: TBC1D24 SLITRK6 S1PR2 ROR1 OSBPL2 HOMER2 FGFR2 FGFR1 TNC DCDC2 And 136 more,

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Hearing Loss Panel Panel

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States. Hearing Loss Panel that also includes the following genes: TCOF1 SERPINB6 SEMA3E SALL1 RPS6KA3 PITX2 MYO7A MYH9 HGF DTD1 And 112 more,

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Ciliopathies Panel

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States. Ciliopathies that also includes the following genes: CFTR B9D1 ZIC3 XPNPEP3 WDR19 USH1C TTC8 TTC21B TSC2 TSC1 And 83 more,

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CDH23 Sequencing Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States.

This panel specifically test the CDH23 gene.

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OtoSeq Hearing Loss Panel by next-generation sequencing (NGS) Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States. OtoSeq Hearing Loss Panel by next-generation sequencing (NGS) that also includes the following genes: EYA1 ADGRV1 USH1C TMC1 MYO6 WHRN GJB2 MYO7A SIX5 SIX1 And 13 more,

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Usher Syndrome Panel by next-generation sequencing Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States. Usher Syndrome Panel by next-generation sequencing that also includes the following genes: WHRN MYO7A USH1C ADGRV1 CLRN1 CDH23 PCDH15 USH2A USH1G

More info about this panel

OtoSeq Hearing Loss Deletion/Duplication Panel Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States. OtoSeq Hearing Loss Deletion/Duplication Panel that also includes the following genes: EYA1 USH1C TMC1 MYO6 GJB2 MYO7A FOXI1 SIX5 SIX1 ADGRV1 And 12 more,

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Usher Syndrome Deletion/Duplication Panel Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States. Usher Syndrome Deletion/Duplication Panel that also includes the following genes: MYO7A USH1C ADGRV1 CLRN1 USH1G CDH23 PCDH15 USH2A

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CDH23 Deletion/duplication analysis Panel

By Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center in United States.

This panel specifically test the CDH23 gene.

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OtoGenome Test for Hearing Loss (87 Genes) Panel

By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine in United States. OtoGenome Test for Hearing Loss (87 Genes) that also includes the following genes: HSD17B4 ATP6V1B1 CIB2 CACNA1D CLRN1 CCDC50 EYA1 GIPC3 GJB2 EDN3 And 76 more,

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Usher Syndrome Panel Panel

By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine in United States. Usher Syndrome Panel that also includes the following genes: CLRN1 WHRN MYO7A ADGRV1 USH1C USH2A USH1G CDH23 PCDH15

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Expanded Hearing Loss Panel, Sequencing (56 Genes) and Deletion/Duplication (53 Genes) Panel

By ARUP Laboratories, Molecular Genetics and Genomics in United States. Expanded Hearing Loss Panel, Sequencing (56 Genes) and Deletion/Duplication (53 Genes) that also includes the following genes: MYO3A LHFPL5 ADGRV1 GJB2 DSPP PJVK COL11A2 CEACAM16 CRYM USH1C And 46 more,

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CDH23. Complete sequencing Panel

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

This panel specifically test the CDH23 gene.

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Audiome (hearing loss panel) Panel

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States. Audiome (hearing loss panel) that also includes the following genes: COL2A1 BCS1L ADGRV1 TMPRSS3 S1PR2 OSBPL2 TBC1D24 SLITRK6 CLPP OTOGL And 96 more,

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Usher syndrome type 1D/F (sequence analysis of CDH23 gene) Panel

By CGC Genetics in Portugal.

This panel specifically test the CDH23 gene.

More info about this panel

Syndromic deafness (NGS panel for 62 genes) Panel

By CGC Genetics in Portugal. Syndromic deafness (NGS panel for 62 genes) that also includes the following genes: ALMS1 COL11A2 COL11A1 COL2A1 COL4A4 COL9A2 EDN3 ABHD12 USH1C TCOF1 And 52 more,

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Non syndromic deafness AR and XL (NGS panel for 56 genes) Panel

By CGC Genetics in Portugal. Non syndromic deafness AR and XL (NGS panel for 56 genes) that also includes the following genes: GPSM2 SMPX SERPINB6 OTOG MARVELD2 TMPRSS3 FOXI1 CIB2 ESRRB HGF And 46 more,

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Syndromic and non syndromic deafness (NGS panel for 127 genes) Panel

By CGC Genetics in Portugal. Syndromic and non syndromic deafness (NGS panel for 127 genes) that also includes the following genes: COL9A2 EDNRB OTOGL EDN3 OTOG EYA1 ESPN FOXI1 WHRN KCNQ4 And 117 more,

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Non syndromic deafness AD, AR and XL (NGS panel for 79 genes) Panel

By CGC Genetics in Portugal. Non syndromic deafness AD, AR and XL (NGS panel for 79 genes) that also includes the following genes: TMPRSS3 TMC2 TMC1 USH1C TNC DSPP DIAPH3 ESPN GIPC3 FOXI1 And 69 more,

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Usher syndrome (NGS panel for 12 genes) Panel

By CGC Genetics in Portugal. Usher syndrome (NGS panel for 12 genes) that also includes the following genes: CIB2 WHRN CLRN1 MYO7A HARS ADGRV1 USH1C PDZD7 CDH23 PCDH15 And 2 more,

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Usher Syndrome Sequencing Panel Panel

By PreventionGenetics PreventionGenetics in United States. Usher Syndrome Sequencing Panel that also includes the following genes: MYO7A ADGRV1 PDZD7 CIB2 USH1C WHRN CLRN1 USH1G CDH23 USH2A And 1 more,

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Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel Panel

By PreventionGenetics PreventionGenetics in United States. Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel that also includes the following genes: TEAD1 ADAMTS18 AHI1 ADIPOR1 ARL3 ALMS1 ABCD1 B9D2 ACO2 ATXN7 And 270 more,

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Usher Syndrome Type 1 and Deafness, Autosomal Recessive 12 (DFNB12) via the CDH23 Gene Panel

By PreventionGenetics PreventionGenetics in United States.

This panel specifically test the CDH23 gene.

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Usher 1 Panel Panel

By FirmaLab in United States. Usher 1 Panel that also includes the following genes: MYO7A USH1C PCDH15 CDH23

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DFNB12 Nonsyndromic Hearing Loss and Deafness Panel

By Bioscientia GmbH Center for Human Genetics in Germany. DFNB12 Nonsyndromic Hearing Loss and Deafness that also includes the following genes: CDH23 ATP2B2

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Usher Syndrome Type 1D Panel

By Bioscientia GmbH Center for Human Genetics in Germany.

This panel specifically test the CDH23 gene.

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Usher syndrome type 1D/F Panel

By Centogene AG - the Rare Disease Company in Germany.

This panel specifically test the CDH23 gene.

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Deafness, non-syndromic sensorineural AR panel Panel

By Centogene AG - the Rare Disease Company in Germany. Deafness, non-syndromic sensorineural AR panel that also includes the following genes: SLC12A1 TECTA MARVELD2 LHFPL5 GPSM2 ESRRB HGF TMC1 MYO6 GIPC3 And 33 more,

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Hearing Loss, nonsyndromic, autosomal recessive and X-linked Panel Panel

By CeGaT GmbH in Germany. Hearing Loss, nonsyndromic, autosomal recessive and X-linked Panel that also includes the following genes: CABP2 COL11A2 ESPN GIPC3 STRC SLITRK6 TMPRSS3 CIB2 HGF OTOG And 43 more,

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Syndromic Hearing Loss Panel Panel

By CeGaT GmbH in Germany. Syndromic Hearing Loss Panel that also includes the following genes: MYO7A ATP6V1B1 ANKH ABHD12 CACNA1D COL4A4 EDNRB CHD7 CDKN1C KCNQ1 And 52 more,

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Usher Syndrome Panel Panel

By CeGaT GmbH in Germany. Usher Syndrome Panel that also includes the following genes: CLRN1 CIB2 ABHD12 MYO7A HARS ADGRV1 WHRN PDZD7 USH1C CDH23 And 5 more,

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Usher Syndrome Panel

By Asper Biogene Asper Biogene LLC in Estonia. Usher Syndrome that also includes the following genes: PDZD7 DSPP TNC ADGRV1 CIB2 HARS MYO7A ABHD12 GIPC3 WHRN And 10 more,

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Sensorineural Hearing Loss Panel

By Asper Biogene Asper Biogene LLC in Estonia. Sensorineural Hearing Loss that also includes the following genes: TRMU DIAPH3 CRYM COL11A2 MYO7A TECTA CIB2 TMC1 MYO6 GJB2 And 67 more,

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Eye diseases comprehensive panel Panel

By Asper Biogene Asper Biogene LLC in Estonia. Eye diseases comprehensive panel that also includes the following genes: GSN VSX1 PITX2 PDZD7 PAX6 OFD1 IMPG2 GDF6 CYP1B1 CEP290 And 265 more,

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Retinal Dystrophy Panel Panel

By Molecular Vision Laboratory in United States. Retinal Dystrophy Panel that also includes the following genes: TEAD1 WDR19 SPP2 ABCD1 C12orf65 IFT81 GJB2 KIF11 IFT172 B9D2 And 277 more,

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USHER syndrome panel Panel

By Molecular Vision Laboratory in United States. USHER syndrome panel that also includes the following genes: HARS CIB2 USH1C ABHD12 CLRN1 WHRN ADGRV1 MYO7A USH1G CEP250 And 4 more,

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CDH23 single gene sequencing Panel

By Molecular Vision Laboratory in United States.

This panel specifically test the CDH23 gene.

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Usher syndrome Panel

By VECMD VECMD in Mexico. Usher syndrome that also includes the following genes: MYO7A USH1C USH2A USH1G CDH23

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Ciliopathy Focus Panel Panel

By Courtagen Diagnostics Laboratory Courtagen Life Sciences in United States. Ciliopathy Focus Panel that also includes the following genes: WDR19 RSPH3 CCNO SPAG1 ARL6 TTC21B ZIC3 CRX BBS10 TMEM216 And 142 more,

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qCarrier Plus Panel

By Quantitative Genomic Medicine Laboratories, SL in Spain. qCarrier Plus that also includes the following genes: ADA ABCD1 BRWD3 SLC22A5 DUOXA2 JAK3 FKRP CLN3 AR COL4A4 And 290 more,

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DEAFNESS A.D. and A.R. Panel

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. DEAFNESS A.D. and A.R. that also includes the following genes: CIB2 CCDC50 GIPC3 GJB2 HGF MYO1A MYO3A MYO6 MYO7A GRHL2 And 45 more,

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DEAFNESS A.R. (39 genes) Panel

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. DEAFNESS A.R. (39 genes) that also includes the following genes: CIB2 GIPC3 GJB2 HGF MYO3A MYO6 MYO7A COL11A2 MARVELD2 SERPINB6 And 28 more,

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USHER SYNDROME and NON-SYNDROMIC DEAFNESS Panel

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain. USHER SYNDROME and NON-SYNDROMIC DEAFNESS that also includes the following genes: MYO7A CLRN1 ADGRV1 MYO6 USH1C TMPRSS3 TMC1 WHRN CDH23 GJB6 And 8 more,

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Eye Disorders: Comprehensive Sequencing and Deletion/Duplication Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. Eye Disorders: Comprehensive Sequencing and Deletion/Duplication Panel that also includes the following genes: EFEMP1 BEST1 OFD1 TPP1 CIB2 COL2A1 MFN2 COL4A1 BMP4 PITX2 And 197 more,

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Usher Syndrome: Sequencing Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. Usher Syndrome: Sequencing Panel that also includes the following genes: CIB2 PDZD7 ADGRV1 CLRN1 USH1C MYO7A HARS ABHD12 WHRN USH1G And 3 more,

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Ciliopathies: Sequencing and Deletion/Duplication Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. Ciliopathies: Sequencing and Deletion/Duplication Panel that also includes the following genes: NODAL LEFTY2 SCNN1B OFD1 CFTR TSC1 TSC2 RPGRIP1L KIF7 KCNJ13 And 102 more,

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Hearing Loss: Sequencing Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States. Hearing Loss: Sequencing Panel that also includes the following genes: SALL1 CIB2 FGFR3 CRYM GJB2 SIX1 KCNQ1 EYA1 TECTA DSPP And 82 more,

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Ciliopathies NGS Panel Panel

By Fulgent Genetics Fulgent Genetics in United States. Ciliopathies NGS Panel that also includes the following genes: NODAL CFTR ARL6 AIPL1 MYO7A CLRN1 CRX DNAH5 ADGRV1 DYNC2H1 And 85 more,

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Eye Disorders NGS Panel Panel

By Fulgent Genetics Fulgent Genetics in United States. Eye Disorders NGS Panel that also includes the following genes: EFEMP1 BEST1 PAX6 FOXC1 PRPH2 BCOR MYOC COL11A1 CLN3 OPTN And 128 more,

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Retinitis Pigmentosa NGS Panel Panel

By Fulgent Genetics Fulgent Genetics in United States. Retinitis Pigmentosa NGS Panel that also includes the following genes: RP9 BEST1 C8orf37 PRPH2 PEX7 GNPTG ARL6 AIPL1 CLRN1 CRX And 78 more,

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Hearing Loss NGS Panel Panel

By Fulgent Genetics Fulgent Genetics in United States. Hearing Loss NGS Panel that also includes the following genes: KCNQ1 KCNE1 SIX1 TCF21 GSTP1 FOXI1 CRYM TMPRSS5 MYO1C MYO1F And 93 more,

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Usher Syndrome NGS Panel Panel

By Fulgent Genetics Fulgent Genetics in United States. Usher Syndrome NGS Panel that also includes the following genes: ABHD12 PDZD7 MYO7A CLRN1 ADGRV1 USH1C WHRN PCDH15 USH1G USH2A And 1 more,

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CDH23 Panel

By Fulgent Genetics Fulgent Genetics in United States.

This panel specifically test the CDH23 gene.

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Comprehensive Hearing Loss and Deafness Panel Panel

By Blueprint Genetics in Finland. Comprehensive Hearing Loss and Deafness Panel that also includes the following genes: ABHD12 ALMS1 ADCY1 ANKH BDP1 BTD HSD17B4 ATP6V1B1 CIB2 BCS1L And 148 more,

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Non-Syndromic Hearing Loss Panel Panel

By Blueprint Genetics in Finland. Non-Syndromic Hearing Loss Panel that also includes the following genes: ADCY1 BDP1 CIB2 CABP2 CCDC50 GIPC3 GJB2 HGF MYO1A MYO3A And 81 more,

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Retinal Dystrophy Panel Panel

By Blueprint Genetics in Finland. Retinal Dystrophy Panel that also includes the following genes: AHI1 ALMS1 B9D2 CACNA2D4 CIB2 BBS4 CERKL BBS10 OFD1 CSPP1 And 171 more,

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Usher Syndrome Panel Panel

By Blueprint Genetics in Finland. Usher Syndrome Panel that also includes the following genes: ABHD12 CIB2 CLRN1 HARS ADGRV1 MYO7A USH1C WHRN PDZD7 CDH23 And 3 more,

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Syndromic Hearing Loss Panel Panel

By Blueprint Genetics in Finland. Syndromic Hearing Loss Panel that also includes the following genes: ABHD12 ALMS1 ANKH BTD ATP6V1B1 CIB2 BCS1L CACNA1D CHD7 CLRN1 And 60 more,

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Usher syndrome, type 1D Panel

By Bioarray in Spain.

This panel specifically test the CDH23 gene.

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CarrierMap Panel

By Recombine in United States. CarrierMap that also includes the following genes: ADA GJB2 PUS1 ATP7A PTS ADAMTS2 ALPL AR ACOX1 RARS2 And 291 more,

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Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Panel

By Otogenetics in United States. Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel that also includes the following genes: TMPRSS5 TCF21 MYO1F MYO1C MTAP MT-TM MT-TL2 MIR183 GSTP1 CEMIP And 119 more,

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DEAFNESS, NONSYNDROMIC SENSORINEURAL (AUTOSOMAL RECESSIVE) Panel

By Laboratorio de Genetica Clinica SL in Spain. DEAFNESS, NONSYNDROMIC SENSORINEURAL (AUTOSOMAL RECESSIVE) that also includes the following genes: USH1C TMPRSS3 MYO7A STRC TMC1 PJVK GJB2 CDH23 GJB6 PCDH15 And 3 more,

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USHER SYNDROME TYPE 1 Panel

By Laboratorio de Genetica Clinica SL in Spain. USHER SYNDROME TYPE 1 that also includes the following genes: USH1C MYO7A USH1G PCDH15 CDH23

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Usher Syndrome Type 1D , Sequencing CDH23 Gene Panel

By Reference Laboratory Genetics in Spain.

This panel specifically test the CDH23 gene.

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