OBO ID: DOID:0110558
Term Name: autosomal dominant nonsyndromic deafness 2A Search Ontology:
Synonyms:
  • autosomal dominant deafness 2A
  • DFNA2A
Definition: An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2. https://www.ncbi.nlm.nih.gov/pubmed/10025409
References:
Ontology: Human Disease   ( DOID:0110558 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 2A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KCNQ4 Deafness, autosomal dominant 2A 600101
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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