OBO ID: DOID:0110471 |
Term Name: | autosomal recessive nonsyndromic deafness 16 | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the STRC gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/11687802 | ||
References: |
|
||
Ontology: | Human Disease (DOID:0110471) |
OTHER autosomal recessive nonsyndromic deafness 16 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
STRC | Deafness, autosomal recessive 16 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.