Terminology Service for NFDI4Health

Usher syndrome type 3B

Go to external page http://purl.obolibrary.org/obo/DOID_0110842


An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

Usher syndrome type 3B

Synonyms
  • USH3B
  • Usher syndrome type IIIB
database cross reference
has obo namespace

disease_ontology

id

DOID:0110842