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Human Disease
autosomal dominant nonsyndromic deafness 37
- Term ID
- DOID:0070601
- Synonyms
-
- autosomal dominant deafness 37
- DFNA37
- Definition
- An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the COL11A1 gene on chromosome 1p21.1. (3)
- References
- Ontology
- Human Disease ( DOID:0070601 )
- is a type of
-
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