CDH23 phenotypes and related 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: ORPHANET,NCBIGENE,OMIM,HGNC.

Top 5 symptoms associated to CDH23 gene



Symptoms // Phenotype % Cases
Hemianopia 67%
Osteoporosis 50%
Visual loss 50%
Autosomal recessive inheritance 50%
Cataract 50%

Other less frequent symptoms

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

50% Depression 50% Fatigue 50% Anxiety 50% Headache 33% Abnormality of the menstrual cycle 33% Male hypogonadism 33% Growth hormone excess 33% Impotence 33% Easy fatigability 33% Pallor 33% Diplopia 33% Progressive visual loss 33% Vertigo 33% Infertility 33% Cranial nerve paralysis 33% Hypokalemia 33% Gynecomastia 33% Hypotension 33% Hypogonadotrophic hypogonadism 33% Blindness 33% Delayed puberty 33% Menstrual irregularities 33% Female hypogonadism 33% Decreased fertility in females 33% Fourth cranial nerve palsy 33% Adrenocorticotropin deficient adrenal insufficiency 33% Decreased fertility in males 33% Central adrenal insufficiency 33% Bitemporal hemianopia 33% Cranial nerve VI palsy 33% Abnormality of the pituitary gland 33% Sudden loss of visual acuity 33% Internal ophthalmoplegia 33% Secondary growth hormone deficiency 33% Abnormality of hair density 33% Heteronymous hemianopia 33% Decreased female libido 33% Oculomotor nerve palsy 33% Hypertension 33% Decreased circulating ACTH level 33% Nausea and vomiting 33% Adrenocorticotropic hormone deficiency 33% Hypogonadism 33% Osteopenia 33% Vomiting 33% Abnormal electroretinogram 33% Erectile abnormalities 33% Hearing impairment 33% Sensorineural hearing impairment 33% Ataxia 33% Rod-cone dystrophy 33% Cerebral cortical atrophy 33% Nyctalopia 33% Abnormality of dental enamel 33% Aplasia/Hypoplasia of the cerebellum 33% Hallucinations 33% Global developmental delay 33% Iris hypopigmentation 33% Schizophrenia 33% High-grade hypermetropia 33% Vestibular dysfunction 33% Scotoma 33% Subcortical cerebral atrophy 33% Vestibular hypofunction 33% Abnormality of cochlea 33% Seizures 33% Ptosis 33% Intellectual disability 16% Galactorrhea 16% Congestive heart failure 16% Weight loss 16% Pericardial effusion 16% Thyroid crisis 16% Abnormal visual field test 16% Euthyroid hyperthyroxinemia 16% Supraventricular arrhythmia 16% Periodic hypokalemic paresis 16% Enlarged pituitary gland 16% Increased thyroid-stimulating hormone level 16% Hyperthyroidism 16% Hyperhidrosis 16% Ventricular arrhythmia 16% Prolactin excess 16% Amenorrhea 16% Palpitations 16% Increased circulating gonadotropin level 16% Anterior hypopituitarism 16% Goiter 16% Pituitary hypothyroidism 16% Prelingual sensorineural hearing impairment 16% Immunodeficiency 16% Pituitary prolactin cell adenoma 16% Vertebral compression fractures 16% Truncal obesity 16% Recurrent skin infections 16% Menorrhagia 16% Striae distensae 16% Glucose intolerance 16% Aseptic necrosis 16% Pituitary adenoma 16% Oligomenorrhea 16% Adrenal hyperplasia 16% Increased circulating ACTH level 16% Bipolar affective disorder 16% Purpura 16% Biconcave vertebral bodies 16% Facial erythema 16% Abdominal obesity 16% Poor wound healing 16% Onychomycosis 16% Metrorrhagia 16% Mood changes 16% Abnormal fear/anxiety-related behavior 16% Alkalosis 16% Psychotic mentation 16% Lipodystrophy 16% Premature ovarian insufficiency 16% Dyspareunia 16% Cardiomyopathy 16% Failure to thrive 16% Visual impairment 16% Kyphosis 16% Skeletal muscle atrophy 16% Abdominal pain 16% Abnormality of the eye 16% Myopathy 16% Diabetes mellitus 16% Bruising susceptibility 16% Lethargy 16% Round face 16% Acne 16% Recurrent fractures 16% Sleep disturbance 16% Edema 16% Thin skin 16% Hirsutism 16% Generalized hirsutism 16% Nephrolithiasis 16% Psychosis 16% Telangiectasia of the skin 16% Generalized hyperpigmentation 16% Venous thrombosis 16% Tremor

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

USHER SYNDROME TYPE 1D

Alternate names

USHER SYNDROME TYPE 1D Is also known as ;

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

  • Abnormality of cochlea
  • Vestibular hypofunction
  • Subcortical cerebral atrophy
  • Scotoma
  • Hemianopia


More info about USHER SYNDROME TYPE 1D

SOURCES: OMIM ORPHANET

PITUITARY ADENOMA, ACTH-SECRETING

Alternate names

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

Description

Cushing 'disease' is a condition associated with increased blood cortisol resulting from adrenocorticotropic hormone (ACTH)-producing pituitary tumors that are resistant to glucocorticoid negative feedback (Bilodeau et al., 2006). ACTH is formed as a precursor from the POMC gene product (OMIM ).See also Cushing 'syndrome' (OMIM ), in which excess cortisol secretion results from adrenocortical pathology.

Most common symptoms of PITUITARY ADENOMA, ACTH-SECRETING

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


More info about PITUITARY ADENOMA, ACTH-SECRETING

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

  • Heteronymous hemianopia
  • Abnormality of hair density
  • Internal ophthalmoplegia
  • Fourth cranial nerve palsy
  • Sudden loss of visual acuity


More info about PROLACTINOMA

SOURCES: ORPHANET OMIM

TSH-SECRETING PITUITARY ADENOMA

Most common symptoms of TSH-SECRETING PITUITARY ADENOMA

  • Thyroid crisis
  • Abnormal visual field test
  • Heteronymous hemianopia
  • Abnormality of hair density
  • Fourth cranial nerve palsy


More info about TSH-SECRETING PITUITARY ADENOMA

SOURCES: ORPHANET

USHER SYNDROME TYPE 1D

Alternate names

USHER SYNDROME TYPE 1D Is also known as ;

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

  • Abnormality of cochlea
  • Vestibular hypofunction
  • Subcortical cerebral atrophy
  • Scotoma
  • Hemianopia


More info about USHER SYNDROME TYPE 1D

SOURCES: OMIM ORPHANET

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: ADSL HBB NEUROD1 RAX COL2A1 COL3A1 STAT1 ELAC2 RB1 EYA4 And 627 more,

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CDH23 Sequence 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 (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 GALT GNPTAB GLDC CHAT LAMA3 CFTR SGCG BCKDHA ELP1 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: FAH GLDC DPYD SERPINA1 SMN1 CBS DBT HBA1 HSD17B4 RAPSN 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: TMPRSS3 CRYM TJP2 CIB2 FOXI1 COL11A2 ACTG1 KARS LARS2 TIMM8A 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: TMEM132E TBX1 TBC1D24 SYNE4 SLITRK6 POLR1C OPA1 NLRP3 NARS2 LOXL3 And 136 more,

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Hearing Loss Panel Panel

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University in United States. Hearing Loss Panel that also includes the following genes: TIMM8A TCOF1 SLC17A8 SERPINB6 SEMA3E SALL4 SALL1 PTPRQ PITX2 NLRP3 And 112 more,

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Ciliopathies Panel

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University in United States. Ciliopathies that also includes the following genes: CFTR XPNPEP3 TMEM67 TMEM216 NPHP3 NEK8 KIF7 WHRN DNAL1 CCDC39 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: TMC1 GJB6 WHRN GJB2 MYO7A USH1G TMPRSS3 OTOF FOXI1 EYA1 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: USH1G WHRN MYO7A USH2A CDH23 USH1C PCDH15 CLRN1 ADGRV1

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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: TMC1 GJB6 GJB2 MYO7A FOXI1 USH1G TMPRSS3 OTOF EYA1 USH1C 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: USH1G MYO7A CDH23 USH1C PCDH15 CLRN1 USH2A ADGRV1

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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: DIAPH1 ACTG1 HSD17B4 CIB2 COCH CCDC50 GIPC3 GJB2 GJB6 MYO7A 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: USH1G WHRN MYO7A USH2A CLRN1 ADGRV1 CDH23 PCDH15 USH1C

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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: TRIOBP SLC26A5 OTOA LHFPL5 HARS2 GJB2 DSPP COL11A2 CRYM TMPRSS3 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 TIMM8A TMPRSS3 EPS8 TBC1D24 SYNE4 SLITRK6 LARS2 OTOGL HARS2 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.

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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 COL4A3 COL2A1 COL4A4 COL9A1 COL4A6 USH1G TFAP2A TIMM8A 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 SERPINB6 MARVELD2 TRIOBP TMPRSS3 FOXI1 COL4A6 CIB2 KARS GJB2 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: EDNRB OTOGL PAX3 EYA4 FOXI1 WHRN KCNQ4 KCNQ1 CD151 LOXHD1 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: TJP2 TMPRSS3 TMC2 TMC1 TSPEAR TRIOBP TNC DIAPH1 DSPP DIAPH3 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 USH1G HARS PDZD7 MYO7A PCDH15 ADGRV1 USH2A USH1C 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 USH1G PDZD7 CIB2 WHRN ADGRV1 CDH23 USH1C USH2A PCDH15 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: JAG1 CTNNA1 MYO7A ACBD5 PRKCG TUBGCP4 RDH11 RAB28 PEX26 OPA1 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 PCDH15 CDH23 USH1C

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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: MARVELD2 LHFPL5 GPSM2 TRIOBP TMC1 LRTOMT GIPC3 PTPRQ OTOF MYO15A 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: PTPRQ COL11A2 GIPC3 OTOF SLITRK6 TMPRSS3 LOXHD1 GJB3 CIB2 COL4A6 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 ANKH CD151 COL4A4 EDNRB CHD7 COL4A3 KCNQ1 KCNE1 GATA3 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: USH1G CIB2 HARS PDZD7 MYO7A WHRN PEX1 PCDH15 USH2A PEX6 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: USH1G DSPP LOXHD1 CIB2 WHRN PDZD7 COL4A6 HARS TNC KARS 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: CRYM GJB3 CIB2 MT-TS1 SERPINB6 PTPRQ CCDC50 SLC17A8 COCH GSDME 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: PAX2 PITX2 GDF6 CACNA1F ITM2B ADAMTS18 ZEB1 SLC4A11 MFRP CRX 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: GJB2 GJB6 B9D2 HGSNAT TUBGCP4 KIAA1549 IMPG2 MFSD8 MT-ND4 PNPLA6 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: USH1G HARS CIB2 WHRN MYO7A C2orf71 CEP250 USH1C ABHD12 CLRN1 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 USH1G USH2A CDH23 USH1C

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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: EVC CCDC28B TMEM67 WDR19 CEP104 MKKS 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: COL7A1 IVD NPC1 BCKDHA GCDH TPP1 FKTN GNPTAB CLCN1 MMADHC 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: ACTG1 CIB2 COCH CCDC50 GIPC3 GJB2 GJB6 MYO7A MYO15A COL11A2 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 GJB6 MYO7A MYO15A COL11A2 OTOF 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 GJB6 OTOF MT-TS1 USH1G TMPRSS3 TMC1 WHRN CDH23 CLRN1 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: OFD1 COL4A1 PITX2 LZTFL1 VSX2 CACNA1F MKKS CEP290 SAG RPE65 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: USH1G HARS WHRN CIB2 PDZD7 MYO7A CLRN1 CDH23 USH1C ABHD12 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: SCNN1G KIF7 NPHP3 MKS1 NPHP4 TULP1 CRB1 ZNF423 DNAL1 XPNPEP3 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 GJB6 GJB2 KCNQ1 ACTG1 DNMT1 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: BBS4 CFTR ALMS1 MKS1 MKKS ZIC3 RPE65 LRAT TMEM216 NEK8 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 MTTP COL9A1 OPA1 MFRP CNGB3 NPHP4 TULP1 RPGRIP1 CRB1 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 CACNA1F MKKS SAG RPE65 WHRN MAK PRPF6 GUCA1B FLVCR1 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: LHX3 TBL1X MYO1F GJB6 PDZD7 COL11A2 GJA1 JAG1 GPSM2 GRXCR1 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: USH1G PDZD7 MYO7A WHRN ABHD12 CDH23 CLRN1 USH1C PCDH15 ADGRV1 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: ACTG1 ALMS1 ANKH BTD HSD17B4 CIB2 CD151 COCH CHD7 CCDC50 And 146 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: ACTG1 CIB2 COCH CCDC50 GIPC3 GJB2 EPS8 GJB6 MYO7A MYO15A 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 CIB2 BBS4 CERKL BBS10 CABP4 OFD1 CRX 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: CIB2 HARS MYO7A USH1G WHRN PDZD7 CDH23 CLRN1 ADGRV1 PCDH15 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: ACTG1 ALMS1 ANKH BTD CIB2 CD151 CHD7 COL4A3 COL9A1 DLX5 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: MTHFR ADAMTS2 ALG6 ALPL AR AGXT ABCD1 IDUA AMH ARG1 And 288 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 TBL1X MYO1F MYO1C MT-TL2 GJB4 CEMIP EDNRA CRYM MT-TL1 And 119 more,

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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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Other genes that you may find interesting

SLC19A2