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PARC syndrome

Disease Summary
Associated Targets (0)

Explore 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.
Mondo Term and Equivalent IDs
MONDO:0010867:  PARC syndrome
GARD:0004223: 
MESH:C537174: 
Orphanet:2825: 
UMLS:C1838256: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found