Search Ontology:
Human Disease
autosomal recessive nonsyndromic deafness 1B
- Term ID
- DOID:0110476
- Synonyms
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- autosomal recessive deafness 1B
- DFNB1B
- Definition
- An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/11807148
- References
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- ICD10CM:H90.3
- MIM:612645
- Ontology
- Human Disease ( DOID:0110476 )
- is a type of
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Genes Involved
Zebrafish Models