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PARC syndrome
Disease Summary
Associated Targets ()
Mondo Description PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990.
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.
GARD:0004223
MESH:C537174
OMIM:600331
Orphanet:2825
UMLS:C1838256
MONDO:0010867
High level summary of knowledge for a disease, including descriptions and datasource references.