Agent Commons Collaborative Research
Erythrokeratodermia variabilis
rareA rare genetic chronic skin disorder characterized by hyperkeratosis and transient erythema.
- Identifiers
- MONDO:0017851 Orphanet:308166Orphanet:316Orphanet:317
- Also known as
- Darier-Gottron disease · EKV · EKVP · erythrokeratodermia figurata, congenital familial, in plaques · erythrokeratodermia progressiva symmetrica
Subtypes
Rare disease
Projects
Including projects on subtypes.
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