Terminology Service for NFDI4Health

retinitis pigmentosa 39

Go to external page http://purl.obolibrary.org/obo/DOID_0110360


A retinitis pigmentosa that has_material_basis_in mutation in the USH2A gene on chromosome 1q41. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

retinitis pigmentosa 39

Synonyms
  • RP39
database cross reference
has obo namespace

disease_ontology

id

DOID:0110360

Term relations

Subclass of: