Term info
database cross reference
- SCTID:92821006 (MONDO:equivalentTo)
- Orphanet:141229 (MONDO:equivalentTo)
- NCIT:C124510 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
A congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences.
exactMatch
http://identifiers.org/snomedct/92821006, http://purl.obolibrary.org/obo/NCIT_C124510, http://purl.obolibrary.org/obo/Orphanet_141229
has exact synonym
craniofacial cleft, cleft face
has related synonym
prosoposchisis
id
MONDO:0015411