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Human Disease

autosomal dominant nonsyndromic deafness 77

Term ID
DOID:0112168
Synonyms
  • DFNA77
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11. https://pubmed.ncbi.nlm.nih.gov/31273342/
References
Ontology
Human Disease   ( DOID:0112168 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models