Overview
Camptodactyly is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Mesomelic dysplasia with cleft palate and camptodactyly syndrome(child)
Camptodactyly with joint contracture and facial skeletal defect syndrome(child)
Tel Hashomer camptodactyly syndrome(child)
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome(child)
CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome(child)
Camptodactyly syndrome Guadalajara type 1(child)
Crisponi syndrome(child)
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome(child)
Arthrogryposis and ectodermal dysplasia syndrome(child)
Hereditary camptodactyly(child)
Camptodactyly of bilateral toes(child)
Camptodactyly of finger(child)
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome(child)
Sporadic camptodactyly(child)
Camptodactyly of right hand(child)
Camptodactyly of left hand(child)
Congenital abnormal shape of digit(parent)
Congenital deformity of musculoskeletal system(parent)
Quick Facts
- SNOMED CT
- 29271008
- UMLS CUI
- C0685409
- Fully Specified Name
- Camptodactyly (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.