PARC syndrome
MONDO:0010867Mondo
Findings
No curated finding names PARC syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0010867), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: PARC syndrome
- Also called
- poikiloderma-alopecia-retrognathism-cleft palate syndrome