OBO ID: DOID:0080269
Term Name: autosomal dominant nonsyndromic deafness 73 Search Ontology:
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:
OTHER autosomal dominant nonsyndromic deafness 73 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PTPRQ Deafness, autosomal dominant 73 617663
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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