Term info
database cross reference
- HP:0001149 (MONDO:otherHierarchy)
- ICD9:277.39 (MONDO:relatedTo)
- UMLS:C0155127 (MONDO:equivalentTo)
- ICD9:357.4 (MONDO:relatedTo)
- SCTID:1192004 (MONDO:equivalentTo)
- DOID:8943 (MONDO:equivalentTo)
IAO 0000589
lattice corneal dystrophy (disease)
comment
Editor note: TODO this class sourced from DO, may contain mistakes; may be confused with Lattice corneal dystrophy type II
exactMatch
http://identifiers.org/snomedct/1192004, http://purl.obolibrary.org/obo/DOID_8943, http://linkedlifedata.com/resource/umls/id/C0155127
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0000764
has exact synonym
familial amyloid neuropathy, Finnish type, lattice corneal dystrophy, lattice corneal dystrophy (disease)
id
MONDO:0004686