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facial cleft
Disease Summary
Associated Targets (4)
Tbio
4
Mondo Description 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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
NCIT:C124510
Orphanet:141229
SCTID:92821006
MONDO:0015411
High level summary of knowledge for a disease, including descriptions and datasource references.