erythrokeratoderma en cocardes
Findings
No curated finding names erythrokeratoderma en cocardes yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Erythrokeratoderma 'en cocardes' is a rare genodermatosis characterized by circumscribed target-like (or 'en cocardes') erythematous hyperkeratotic lesions. These lesions, which remit and recur, affect the trunk and extremities and are accompanied by scaly plaques evocative of erythrokeratoderma variabilis. Onset usually occurs at birth or during early childhood. Only few cases have been described. Transmission is autosomal dominant.
Definition from the Mondo Disease Ontology (MONDO:0017836), read 2026-09-29. CC BY 4.0.
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal skin pigmentationHPOHP:0001000
- Very frequent (80% to 99% of cases)
- HyperkeratosisHPOHP:0000962
- Very frequent (80% to 99% of cases)
- Neoplasm of the skinHPOHP:0008069
- Very frequent (80% to 99% of cases)
- PapuleHPOHP:0200034
- Very frequent (80% to 99% of cases)
- NeoplasmHPOHP:0002664
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
2 names
Resolves to: erythrokeratoderma en cocardes
- Also called
- Degos genodermatosisDegos genodermatosis "en cocardes"