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.
Lenz-Majewski hyperostosis syndrome
Dubowitz's syndrome
Occasional (5-29%)
Coffin-Siris syndrome
Coffin-Lowry syndrome
Primary hyperoxaluria
Very rare (1-4%)
Cystathionine beta-synthase deficiency
Adams-Oliver syndrome
Very frequent (80-99%)
De Lange syndrome
Frequent (30-79%)
Smith-Lemli-Opitz syndrome
Frequent (30-79%)
Medionecrosis of aorta
Very frequent (80-99%)
Congenital muscular hypertrophy-cerebral syndrome
Hypersensitivity angiitis
Very frequent (80-99%)
Primary hyperoxaluria, type I
Sarcoidosis, lupus pernio type
Frequent (30-79%)
Allergic granulomatosis angiitis
Occasional (5-29%)
Polyarteritis nodosa
Occasional (5-29%)
Cryoglobulinaemic vasculitis
Very frequent (80-99%)
Macroglobulinaemia
Occasional (5-29%)
Waldenstrom's macroglobulinemia
Occasional (5-29%)
Aicardi Goutieres syndrome
Occasional (5-29%)
Bannayan syndrome
Occasional (5-29%)
Calciphylaxis
Very frequent (80-99%)
Idiopathic livedo reticularis with summer ulceration
Frequent (30-79%)
Idiopathic livedo reticularis with systemic involvement
Very frequent (80-99%)
Chilblain lupus erythematosus
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 26825009
- UMLS CUI
- C0263401
- Fully Specified Name
- Cutis marmorata (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.