C84696Level 6
Erythrokeratodermia Variabilis
**Semantic type:** Disease or Syndrome
**Definition:** A rare genetic chronic skin disorder characterized by hyperkeratosis and transient erythema. Mutations in GJB3 and GJB4 genes have been identified as causative agents.
**Synonyms:** - Erythrokeratodermia Variabilis et Progressiva
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