Overview
Craniofacial conodysplasia 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.
Anomaly of the face
Very frequent (80-99%)HP:0000271
Cone-shaped epiphyses of the fingers
Very frequent (80-99%)HP:0010230
Craniofacial dysostosis
Very frequent (80-99%)HP:0004439
Nonsyndromal hydrocephalus
Very frequent (80-99%)HP:0000238
Spinal cord compression
Very frequent (80-99%)HP:0002176
Related Conditions
Autosomal dominant hereditary disorder(parent)
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Congenital anomaly of face bones(parent)
Congenital anomaly of skull(parent)
Skeletal dysplasia(parent)
Hereditary disorder of musculoskeletal system(parent)
Lesion of face(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 720754008
- UMLS CUI
- C4303862
- Fully Specified Name
- Craniofacial conodysplasia syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 5
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.