Deafness, Autosomal Dominant 71; Dfna71
Genes related to Deafness, Autosomal Dominant 71; Dfna71
Clinical FeaturesPhenotypes 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 researchersCurrently, 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
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
By Fulgent Genetics Fulgent Genetics (United States).
You can get up to -5 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.OMIM Rare Disease Search Engine
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LAURENCE-MOON SYNDROME; LNMS IMMUNODEFICIENCY 12; IMD12 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39; EIEE39 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31; COXPD31 AICARDI-GOUTIÈRES SYNDROME FAMILIAL PANCREATIC CARCINOMA