Overview
Hecht Scott 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.
Abnormal fibula morphology
Very frequent (80-99%)HP:0002991
Abnormal tibia morphology
Very frequent (80-99%)HP:0002992
Absent hand
Very frequent (80-99%)HP:0004050
Cardiovascular disease
Frequent (30-79%)HP:0001626
Decreased body height
Frequent (30-79%)HP:0004322
Partial syndactyly
Frequent (30-79%)HP:0006101
Premature birth
Frequent (30-79%)HP:0001622
Respiratory insufficiency
Frequent (30-79%)HP:0002093
Split hand
Frequent (30-79%)HP:0001171
Tarsal bone synostosis
Frequent (30-79%)HP:0008368
Abnormal hands
HP:0001155
Absent fibulae
HP:0002990
Absent fingers
HP:0009380
Missing toes
HP:0001849
Short skankbone
HP:0005736
Syndactyly
HP:0001159
Tibial bowing
HP:0002982
Quick Facts
- SNOMED CT
- 783156008
- UMLS CUI
- C1855499
- Fully Specified Name
- Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.