Term info
- DOID:0080085 (MONDO:equivalentTo)
- Orphanet:79144 (OMIM:605779)
- SCTID:403281007 (MONDO:equivalentTo)
- UMLS:C1853984 (Orphanet:79144)
- OMIM:605779 (Orphanet:79144/e)
- MESH:C538333 (MONDO:equivalentTo)
- GARD:0009761 (MONDO:equivalentTo)
ordo_disease
https://github.com/monarch-initiative/mondo/issues/4069
Editor note: Orphanet classifies as both syndromic and isolated. See https://github.com/monarch-initiative/mondo-build/issues/49
https://omim.org/entry/605779, http://purl.obolibrary.org/obo/DOID_0080085, http://purl.obolibrary.org/obo/Orphanet_79144, http://linkedlifedata.com/resource/umls/id/C1853984, http://identifiers.org/snomedct/403281007, http://identifiers.org/mesh/C538333
COIF syndrome, COIF, Iso-Kikuchi syndrome, congenital onychodysplasia of the index fingers, nonsyndromic congenital nail disorder type 7
congenital isolated nail dysplasia, NDNC7, onychodysplasia, isolated congenital, isolated congenital nail dysplasia, nail dysplasia, isolated congenital, isolated congenital onychodysplasia, nail disorder, nonsyndromic congenital, 7
MONDO:0011595