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Human Disease

autosomal dominant nonsyndromic deafness 81

Term ID
DOID:0070608
Synonyms
  • autosomal dominant deafness 81
  • DFNA81
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ELMOD3 gene on chromosome 2p11. https://pubmed.ncbi.nlm.nih.gov/29713870/
References
Ontology
Human Disease   ( DOID:0070608 )
Relationships
is a type of
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Genes Involved
Zebrafish Models