Metadata | |
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ID | DOID:0110488 |
Name | autosomal recessive nonsyndromic deafness 3 |
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 MYO15A gene on chromosome 17p11. https://www.ncbi.nlm.nih.gov/pubmed/17851452 |
Xrefs | |
Synonyms |
autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3 [EXACT] DFNB3 [EXACT] NRSD3 [EXACT] |
Parent Relationships |