Overview
PARC syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Absent eyebrows
Always present (100%)HP:0002223
Absent eyelashes
Always present (100%)HP:0000561
Cleft of palate
Always present (100%)HP:0000175
Hair loss
Always present (100%)HP:0001596
Poikiloderma
Always present (100%)HP:0001029
Retromicrognathia
Always present (100%)HP:0000308
Related Conditions
Multiple system malformation syndrome(parent)
Hereditary disorder of the integument(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital alopecia(parent)
Cleft palate(parent)
Congenital retrognathism(parent)
Autosomal dominant hereditary disorder(parent)
Poikiloderma(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 771186004
- UMLS CUI
- C1838256
- Fully Specified Name
- Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 6
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.