Terminology Service for NFDI4Health

retinitis pigmentosa 49

Go to external page http://purl.obolibrary.org/obo/DOID_0110377


A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

retinitis pigmentosa 49

Synonyms
  • RP49
database cross reference
has obo namespace

disease_ontology

id

DOID:0110377

Term relations

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