OBO ID: DOID:0080267
Term Name: autosomal dominant nonsyndromic deafness 71 Search Ontology:
Synonyms:
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the DMXL2 gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/27657680/
References:
Ontology: Human Disease   (DOID:0080267)
OTHER autosomal dominant nonsyndromic deafness 71 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DMXL2 ?Deafness, autosomal dominant 71 617605
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None