Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group of pigmentary retinopathies. [ Orphanet:1872 ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIMPS:120970 (MONDO:equivalentTo)
  • GARD:0010790 (Orphanet-shared)
  • DOID:0050572 (MONDO:equivalentTo)
  • Orphanet:1872 (MONDO:equivalentTo)
  • ICD10:H35.5 (Orphanet:1872)
Subsets

ordo_disease

definition

Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group of pigmentary retinopathies.

exactMatch

http://purl.obolibrary.org/obo/DOID_0050572

http://www.orpha.net/ORDO/Orphanet_1872

has exact synonym

cone-rod retinal dystrophy

has related synonym

cone rod dystrophy

id

MONDO:0015993

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml