Search Ontology:
Human Disease
Usher syndrome type 3B
- Term ID
- DOID:0110842
- Synonyms
-
- USH3B
- Usher syndrome type IIIB
- Definition
- An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. https://www.ncbi.nlm.nih.gov/pubmed/22279524
- References
-
- ICD10CM:H35.5
- MIM:614504
- Ontology
- Human Disease ( DOID:0110842 )
- is a type of
-
- inverse disjoint_from
-
Other Pages
Genes Involved
Zebrafish Models