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Human Disease

autosomal dominant nonsyndromic deafness 72

Term ID
DOID:0080268
Synonyms
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SLC44A4 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28013291/
References
Ontology
Human Disease   ( DOID:0080268 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models