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autosomal dominant keratitis

Go to external page http://purl.obolibrary.org/obo/MONDO_0007848

Hereditary keratitis is characterized by opacification and vascularisation of the cornea, often associated with macula hypoplasia. [ Orphanet:2334 ]

Synonyms: hereditary keratitis keratitis, autosomal dominant

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:3089 (MONDO:GARD)
  • UMLS:C1835698 (MONDO:equivalentTo)
  • OMIM:148190 (Orphanet:2334/e)
  • Orphanet:2334 (OMIM:148190)
  • SCTID:715339004 (MONDO:equivalentTo)
  • DOID:0111383 (MONDO:equivalentTo)
  • MEDGEN:332039 (MONDO:equivalentTo)
  • MESH:C537022 (Orphanet:2334/e)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

exactMatch

http://linkedlifedata.com/resource/umls/id/C1835698

http://purl.obolibrary.org/obo/DOID_0111383

http://www.orpha.net/ORDO/Orphanet_2334

https://omim.org/entry/148190

http://identifiers.org/mesh/C537022

http://identifiers.org/medgen/332039

http://identifiers.org/snomedct/715339004

has related synonym

keratitis, hereditary

dominantly inherited keratitis

id

MONDO:0007848