Overview
Brachydactyly elbow wrist dysplasia 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 distal phalanx morphology of finger
Very frequent (80-99%)HP:0009832
Abnormal humerus morphology
Very frequent (80-99%)HP:0031095
Abnormal morphology of ulna
Very frequent (80-99%)HP:0040071
Abnormality of the fingernails
Very frequent (80-99%)HP:0001231
Absent/underdeveloped radius
Very frequent (80-99%)HP:0006501
Big calvaria
Very frequent (80-99%)HP:0000256
Brachydactyly
Very frequent (80-99%)HP:0001156
Elbow dislocation
Very frequent (80-99%)HP:0003042
Fusion of wrist bones
Very frequent (80-99%)HP:0005048
Permanent curving of the pinkie finger
Very frequent (80-99%)HP:0004209
Stiff joint
Very frequent (80-99%)HP:0001387
2-3 finger cutaneous syndactyly
HP:0001233
Anomalous carpal bones
HP:0001191
Fixed flexion at the elbow joint
HP:0002987
Joint contracture of the 5th finger
HP:0009183
Radially deviated wrists
HP:0006190
Widened metaphyses
HP:0003016
Related Conditions
Autosomal dominant hereditary disorder(parent)
Brachydactyly(parent)
Congenital anomaly of upper limb(parent)
Congenital anomaly of joint(parent)
Lesion of joint(parent)
Hereditary disorder of musculoskeletal system(parent)
Arthropathy of wrist(parent)
Arthropathy of elbow(parent)
Skeletal dysplasia(parent)
Developmental hereditary disorder(parent)
Congenital dysplasia of limb(parent)
Quick Facts
- SNOMED CT
- 764437006
- UMLS CUI
- C1861313
- Fully Specified Name
- Brachydactyly elbow wrist dysplasia (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.