Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bd0903d926019a6bf3f697f4ccdc1f01d> ?p ?o ?g. }
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- Bd0903d926019a6bf3f697f4ccdc1f01d hasDbXref "Orphanet:1517" @default.
- Bd0903d926019a6bf3f697f4ccdc1f01d type Axiom @default.
- Bd0903d926019a6bf3f697f4ccdc1f01d annotatedProperty IAO_0000115 @default.
- Bd0903d926019a6bf3f697f4ccdc1f01d annotatedSource MONDO_0009406 @default.
- Bd0903d926019a6bf3f697f4ccdc1f01d annotatedTarget "Cantu syndrome is a rare disorder characterized by congenital hypertrichosis, osteochondrodysplasia, cardiomegaly, and dysmorphism." @default.