Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 89

Term ID
DOID:0070612
Synonyms
  • autosomal dominant deafness 89
  • DFNA89
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ATOH1 gene on chromosome 4q22. https://pubmed.ncbi.nlm.nih.gov/33111345/
References
Ontology
Human Disease   ( DOID:0070612 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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