Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bd07c7db09adfcee48ee10826c32142c8> ?p ?o ?g. }
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- Bd07c7db09adfcee48ee10826c32142c8 hasDbXref "Orphanet:1667" @default.
- Bd07c7db09adfcee48ee10826c32142c8 type Axiom @default.
- Bd07c7db09adfcee48ee10826c32142c8 annotatedProperty IAO_0000115 @default.
- Bd07c7db09adfcee48ee10826c32142c8 annotatedSource MONDO_0009192 @default.
- Bd07c7db09adfcee48ee10826c32142c8 annotatedTarget "Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure." @default.