Overview
Hypochondrogenesis 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.
Abdominal protuberance
Always present (100%)HP:0001538
Delayed tibial epiphyseal ossification
Always present (100%)HP:6000867
Frontal protuberance
Always present (100%)HP:0002007
Increased length of philtrum
Always present (100%)HP:0000343
Large eyeballs
Always present (100%)HP:0001090
Retromicrognathia
Always present (100%)HP:0000308
shortened long tubular bones
Always present (100%)HP:0003026
Wide cranium shape
Always present (100%)HP:0000248
Abnormality of the feet
HP:0001760
Absent vertebral body mineralization
HP:0004605
Barrel chest
HP:0001552
Cleft of palate
HP:0000175
Crescent-shaped iliac wing
HP:6000653
Cystic hygroma of the neck
HP:0000476
Delayed distal femoral epiphyseal ossification
HP:6000866
Dwarfism, short-limbed
HP:0008873
Horizontal ribs
HP:0000888
Hydramnios
HP:0001561
Hydrops fetalis
HP:0001789
Hypoplastic iliac wing
HP:0002866
Short ribs
HP:0000773
Short-trunked dwarfism
HP:0003521
Shortened long tubular bones of the hand
HP:0001248
Soft tissue swelling
HP:0000969
Widened long bones
HP:0005622
Related Conditions
Quick Facts
- SNOMED CT
- 205483007
- UMLS CUI
- C0542428
- Fully Specified Name
- Hypochondrogenesis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.