Terminology Service for NFDI4Health

retinitis pigmentosa 38

Go to external page http://purl.obolibrary.org/obo/DOID_0110367


A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

retinitis pigmentosa 38

Synonyms
  • RP38
database cross reference
has obo namespace

disease_ontology

id

DOID:0110367