Search Ontology:
Human Disease
autosomal dominant nonsyndromic deafness 71
- Term ID
- DOID:0080267
- 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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models