Overview
Hecht 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.
Lockjaw
Always present (100%)HP:0000211
Decreased body height
Very frequent (80-99%)HP:0004322
Limitation of joint mobility
Very frequent (80-99%)HP:0001376
Muscular abnormality
Very frequent (80-99%)HP:0003011
Big calvaria
Occasional (5-29%)HP:0000256
Dislocated femoral heads
Occasional (5-29%)HP:0002827
Eye drop
Occasional (5-29%)HP:0000508
Increased size of mandible
Occasional (5-29%)HP:0000303
Long lower third of face
Occasional (5-29%)HP:0400000
Prominent philtrum
Occasional (5-29%)HP:0002002
Arthrogryposis multiplex
HP:0002804
Decreased projection of mandible
HP:0000347
Deglutition disorder
HP:0002015
Distal arthrogryposis
HP:0005684
Feeding difficulties
HP:0011968
Fetal foot inversion
HP:0001762
Hammertoe
HP:0001765
Sickled feet
HP:0001840
Unbalanced face
HP:0000324
Webbed skin of toes
HP:0010621
Quick Facts
- SNOMED CT
- 8757006
- UMLS CUI
- C0265226
- Fully Specified Name
- Hecht syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.