PARC syndrome https://rarediseases.info.nih.gov/diseases/4223/parc-syndrome https://www.malacards.org/card/parc_syndrome UMLS:C1838256 OMIM:600331 MONDO:0010867 MESH:C537174 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. MEDGEN:373923 PARC syndrome GARD:0004223 poikiloderma-alopecia-retrognathism-cleft palate syndrome poikiloderma, alopecia, retrognathism, and cleft palate Orphanet:2825 multiple congenital anomalies/dysmorphic syndrome without intellectual disability