Deafness, Autosomal Dominant 69; Dfna69

Clinical Features

Phenotypes and symptoms related to Deafness, Autosomal Dominant 69; Dfna69

  • Hearing impairment
  • Sensorineural hearing impairment
  • Congenital sensorineural hearing impairment
  • Vestibular dysfunction
  • Blue irides
  • Fair hair

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Deafness, Autosomal Dominant 69; Dfna69 Is also known as deafness, congenital, unilateral or asymmetric, dcua.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Deafness, Autosomal Dominant 69; Dfna69 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
OtoSCOPE.

By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics (United States).

ROR1, SIX1, SIX5, SLC22A4, SNAI2, SMPX, SOX10, TBX1, TWNK, TCOF1, TECTA, TIMM8A, TJP2, TMPRSS3, USH1C, USH2A, CLRN1, TSPEAR, WFS1, ESPN , (...)

View the complete list with 130 more genes
Specificity
1 %
Genes
100 %
OtoGenome Test for Hearing Loss (110 Genes).

By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine (United States).

BCS1L, SIX1, SNAI2, SMPX, SOX10, TECTA, TIMM8A, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN, CLIC5, CDH23, CABP2, RIPOR2, CACNA1D, ACTG1, PCDH15 , (...)

View the complete list with 89 more genes
Specificity
1 %
Genes
100 %
Deafness, Autosomal Dominant 69 (DFNA69), and Familial Progressive Hyperpigmentation with or without Hypopigmentation via KITLG Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

KITLG
Specificity
100 %
Genes
100 %
Hypopigmentation Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SNAI2, SOX10, TYR, TYRP1, HPS3, HPS4, SLC45A2, HPS5, DTNBP1, HPS6, LYST, GPR143, SLC24A5, BLOC1S3, LRMDA, MLPH, EDN3, EDNRB, SLC38A8, HPS1 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
100 %
Genetic disorders with abnormal pigmentation Panel.

By CeGaT GmbH (Germany).

BLM, SLC40A1, SNAI2, SOX10, STK11, TFR2, POFUT1, HAMP, ADAM10, LYST, SPRED1, ADAR, POGLUT1, EPG5, MLPH, EDN3, EDNRB, ENPP1, ABCB6, HFE , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
100 %
KIT D816 Mutation Analysis.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti (United States).

KITLG
Specificity
100 %
Genes
100 %
KITLG.

By Fulgent Genetics Fulgent Genetics (United States).

KITLG
Specificity
100 %
Genes
100 %
Neurofibromatosis Panel.

By Blueprint Genetics (Finland).

SMARCB1, SPRED1, KIT, KITLG, NF1, NF2, PTPN11, RAF1
Specificity
13 %
Genes
100 %

You can get up to 3 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

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