Overview
Upington disease 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.
Arthralgias
Frequent (30-79%)HP:0002829
Broad femoral neck
Frequent (30-79%)HP:0006429
Enchondroma
Frequent (30-79%)HP:0030038
Flat capital femoral epiphyses
Frequent (30-79%)HP:0003370
Premature epimetaphyseal fusion
Frequent (30-79%)HP:0010588
Flat head of thigh bone
HP:0008812
Hip arthralgia
HP:0003365
Multiple enchondromatosis
HP:0005701
Related Conditions
Autosomal dominant hereditary disorder(parent)
Congenital hip dysplasia(parent)
Disorganised development of cartilaginous and fibrous components of the skeleton(parent)
Connective tissue hereditary disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Osteochondropathy(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 719041000
- UMLS CUI
- C1860596
- Fully Specified Name
- Hip dysplasia with enchondromata and ecchondroma syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.