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- B99da77780b2a27b652fc85e1a7fe3ff1 hasDbXref "Orphanet:315" @default.
- B99da77780b2a27b652fc85e1a7fe3ff1 type Axiom @default.
- B99da77780b2a27b652fc85e1a7fe3ff1 annotatedProperty IAO_0000115 @default.
- B99da77780b2a27b652fc85e1a7fe3ff1 annotatedSource MONDO_0017836 @default.
- B99da77780b2a27b652fc85e1a7fe3ff1 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.