Deafness, Autosomal Dominant 71; Dfna71
Table of contents:
Clinical Features
Phenotypes and symptoms related to Deafness, Autosomal Dominant 71; Dfna71
- Hearing impairment
- Vestibular dysfunction
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.
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 71; Dfna71 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Ataxia Exome Panel.
By Genetic Services Laboratory University of Chicago (United States).
BCS1L, RTN2, SACS, SCN1A, SCN2A, SCN8A, SCO1, SDHA, SDHD, SLC16A2, SLC17A5, SLC19A2, SLC1A3, SLC20A2, SLC2A1, SLC6A1, SLC9A1, SLC9A6, SNAP25, SOD1 , (...)
View the complete list with 457 more genes
Specificity
1 %
Genes
100 % |
Ataxia and differential diagnoses Panel.
By CeGaT GmbH (Germany).
RPIA, SACS, ATXN1, ATXN10, ATXN2, ATXN7, SCN2A, SLC17A5, SLC1A3, SLC6A1, SLC9A1, SNAP25, BTD, SPG7, SPR, SPTBN2, STUB1, TBP, TWNK, ACO2 , (...)
View the complete list with 184 more genes
Specificity
1 %
Genes
100 % |
DMXL2.
By Fulgent Genetics Fulgent Genetics (United States).
DMXL2
Specificity
100 %
Genes
100 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like IMMUNODEFICIENCY 46; IMD46 ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1; DRS1 CONGENITAL MYOPATHY WITH MYASTHENIC-LIKE ONSET MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18 COUMARIN RESISTANCE COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2