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Human Disease

autosomal dominant nonsyndromic deafness 73

Term ID
DOID:0080269
Synonyms
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the PTPRQ gene on chromosome 12q21. https://pubmed.ncbi.nlm.nih.gov/29309402/
References
Ontology
Human Disease   ( DOID:0080269 )
Relationships
is a type of
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Genes Involved
Zebrafish Models