An instance of retinal degeneration that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: retinal dystrophy retinal degeneration familial retinal dystrophy genetic retinal dystrophy inherited retinal dystrophy hereditary retinal degeneration hereditary retinal dystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:41799005 (MONDO:equivalentTo)
  • SCTID:314407005 (MONDO:equivalentTo)
  • MeSH:D058499
  • DOID:8500 (MONDO:equivalentTo)
  • ICD9:362.75 (i2s)
  • NCIT:C35625 (MONDO:equivalentTo)
  • NCIT:C35194 (MONDO:equivalentTo)
  • ICD9:362.7 (DOID:8500)
  • ICD9:362.70 (i2s)
  • ICD9:362.72 (i2s)
  • MESH:D058499 (Orphanet:71862)
  • OMIM:610125
  • ICD10:H35.50 (DOID:8500)
  • MedDRA:10038857 (Orphanet:71862)
  • MONDO:0019118
  • HP:0000556 (MONDO:otherHierarchy)
  • DOID:8501 (MONDO:equivalentTo)
  • ICD10:H35.5 (MONDO:equivalentTo)
  • UMLS:C0154860 (NCIT:C35194)
  • UMLS:C0854723 (Orphanet:71862)
Subsets

disease_grouping, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10038857

comment

Editor note: This class deliberately merges distinct concepts of RD and inherited RD in other ontologies, as we believe these the same

exactMatch

http://purl.obolibrary.org/obo/NCIT_C35194

http://linkedlifedata.com/resource/umls/id/C0854723

http://identifiers.org/snomedct/41799005

http://purl.obolibrary.org/obo/NCIT_C35625

http://purl.obolibrary.org/obo/DOID_8501

http://purl.obolibrary.org/obo/DOID_8500

http://identifiers.org/mesh/D058499

http://identifiers.org/snomedct/314407005

http://purl.obolibrary.org/obo/Orphanet_71862

http://linkedlifedata.com/resource/umls/id/C0154860

has broad synonym

fundus dystrophy

id

Orphanet:71862