Search Ontology:
Human Disease
autosomal dominant nonsyndromic deafness 13
- Term ID
- DOID:0110545
- Synonyms
-
- autosomal dominant deafness 13
- DFNA13
- Definition
- An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/10581026
- References
-
- ICD10CM:H90.3
- MIM:601868
- Ontology
- Human Disease ( DOID:0110545 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models