OBO ID: DOID:0112160
Term Name: autosomal dominant nonsyndromic deafness 79 Search Ontology:
Synonyms:
  • DFNA79
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22. https://pubmed.ncbi.nlm.nih.gov/31972369/
References:
Ontology: Human Disease   ( DOID:0112160 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 79 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SCD5 ?Deafness, autosomal dominant 79
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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