Overview
Brachydactyly type A3 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.
5th finger middle phalangeal hypoplasia
HP:0004220
Cone-shaped epiphyses
HP:0010579
Curvature of little finger
HP:0004209
Rhomboid or triangular shaped fifth finger middle phalanx
HP:0005910
Type A brachydactyly
HP:0009370
Related Conditions
Autosomal dominant hereditary disorder(parent)
Brachydactyly(parent)
Hereditary disorder of musculoskeletal system(parent)
Longitudinal deficiency of part of upper limb(parent)
Developmental hereditary disorder(parent)
Abnormally short little finger(parent)
Abnormally short phalanx of finger(parent)
Abnormality of middle phalanx morphology of little finger(parent)
Quick Facts
- SNOMED CT
- 890438002
- UMLS CUI
- C1862140
- Fully Specified Name
- Brachydactyly type A3 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 5
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.