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- B2e7ec5dfab21ca2f268eb711c85556b1 hasDbXref "Orphanet:315" @default.
- B2e7ec5dfab21ca2f268eb711c85556b1 type Axiom @default.
- B2e7ec5dfab21ca2f268eb711c85556b1 annotatedProperty IAO_0000115 @default.
- B2e7ec5dfab21ca2f268eb711c85556b1 annotatedSource MONDO_0017836 @default.
- B2e7ec5dfab21ca2f268eb711c85556b1 annotatedTarget "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." @default.