Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Bardet-Biedl syndrome
Hallermann-Streiff syndrome
Necrobiosis lipoidica
Occasional (5-29%)
Fabry's disease
Ehlers-Danlos syndrome, hydroxylysine-deficient
Occasional (5-29%)
Poland anomaly
Frequent (30-79%)
Hidrotic ectodermal dysplasia syndrome
Cholestanol storage disease
Occasional (5-29%)
Farber's lipogranulomatosis
Occasional (5-29%)
Isaacs syndrome
Acute febrile neutrophilic dermatosis
Frequent (30-79%)
Wilson's disease
Very frequent (80-99%)
Lichen myxedematosus
Frequent (30-79%)
Deficiency of melibiase
Westphal-Strumpell syndrome
Very frequent (80-99%)
Troyer syndrome
Frequent (30-79%)
Laurence-Moon syndrome
Acroerythrokeratoderma
Very frequent (80-99%)
Dermochondrocorneal dystrophy
Very frequent (80-99%)
Neuromyotonia
Scleromyxoedema
Frequent (30-79%)
Mycetoma
Occasional (5-29%)
Juvenile seronegative polyarthritis
Occasional (5-29%)
Episodic ataxia type 1
Mesomelic dysplasia Savarirayan type
Excluded (<1%)
Quick Facts
- SNOMED CT
- 299033004
- UMLS CUI
- C0018564
- Fully Specified Name
- Deformity of hand (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.