Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B644ca7cc63f9f479624bda9d9e84ab20> ?p ?o ?g. }
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- B644ca7cc63f9f479624bda9d9e84ab20 hasDbXref "Orphanet:2897" @default.
- B644ca7cc63f9f479624bda9d9e84ab20 type Axiom @default.
- B644ca7cc63f9f479624bda9d9e84ab20 annotatedProperty IAO_0000115 @default.
- B644ca7cc63f9f479624bda9d9e84ab20 annotatedSource MONDO_0008251 @default.
- B644ca7cc63f9f479624bda9d9e84ab20 annotatedTarget "A rare chronic papulosquamous disorder of unknown etiology characterized by small follicular papules, scaly red-orange patches, and palmoplantar hyperkeratosis, which may progress to plaques or erythroderma. Although most of the cases are sporadic and acquired, a familial form of the disease exists." @default.