Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc0fd55d70f2202a25f8b815960c0f4e8> ?p ?o ?g. }
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- Bc0fd55d70f2202a25f8b815960c0f4e8 hasDbXref "Orphanet:444" @default.
- Bc0fd55d70f2202a25f8b815960c0f4e8 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- Bc0fd55d70f2202a25f8b815960c0f4e8 type Axiom @default.
- Bc0fd55d70f2202a25f8b815960c0f4e8 annotatedProperty IAO_0000115 @default.
- Bc0fd55d70f2202a25f8b815960c0f4e8 annotatedSource MONDO_0018631 @default.
- Bc0fd55d70f2202a25f8b815960c0f4e8 annotatedTarget "A rare autosomal dominant hair loss disorder characterized by the absence or scarcity of scalp hair, eyebrows, and eyelashes at birth; coarse and wiry hair during childhood; and progressive hair loss beginning around puberty." @default.