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.
Friedreich's ataxia
Frequent (30-79%)
4p partial monosomy syndrome
Frequent (30-79%)
Adult hypophosphatasia
Townes syndrome
Frequent (30-79%)
Phytanic acid storage disease
Very frequent (80-99%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Occasional (5-29%)
Dextrocardia
Very rare (1-4%)
Fanconi pancytopenia syndrome
Occasional (5-29%)
Ehlers-Danlos syndrome, type 3
Very frequent (80-99%)
Sialic acid storage disease, severe infantile type
Nevus comedonicus
Occasional (5-29%)
Hidrotic ectodermal dysplasia syndrome
Miller syndrome
Farber's lipogranulomatosis
Occasional (5-29%)
Escobar syndrome
Frequent (30-79%)
Accessory navicular bone of foot
Kozlowski spondylometaphyseal dysplasia
20p partial trisomy syndrome
Frequent (30-79%)
Hypochondrogenesis
Gorlin-Chaudhry-Moss syndrome
Very frequent (80-99%)
Troyer syndrome
Frequent (30-79%)
Hennekam lymphangiectasia-lymphoedema syndrome
Occasional (5-29%)
Idiopathic livedo reticularis with summer ulceration
Occasional (5-29%)
Acroerythrokeratoderma
Very frequent (80-99%)
Achondrogenesis, type II
Quick Facts
- SNOMED CT
- 229844004
- UMLS CUI
- C0016506
- Fully Specified Name
- Deformity of foot (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.