Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0176bd129298b8e4fbb8ca4433b0768a> ?p ?o ?g. }
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- B0176bd129298b8e4fbb8ca4433b0768a hasDbXref "Orphanet:2884" @default.
- B0176bd129298b8e4fbb8ca4433b0768a type Axiom @default.
- B0176bd129298b8e4fbb8ca4433b0768a annotatedProperty IAO_0000115 @default.
- B0176bd129298b8e4fbb8ca4433b0768a annotatedSource MONDO_0008244 @default.
- B0176bd129298b8e4fbb8ca4433b0768a annotatedTarget "Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes." @default.