Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B925053b393c2eb1f0b31e500c0ea3fd0> ?p ?o ?g. }
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- B925053b393c2eb1f0b31e500c0ea3fd0 hasDbXref "Orphanet:2166" @default.
- B925053b393c2eb1f0b31e500c0ea3fd0 type Axiom @default.
- B925053b393c2eb1f0b31e500c0ea3fd0 annotatedProperty IAO_0000115 @default.
- B925053b393c2eb1f0b31e500c0ea3fd0 annotatedSource MONDO_0009921 @default.
- B925053b393c2eb1f0b31e500c0ea3fd0 annotatedTarget "Holoprosencephaly-postaxial polydactyly syndrome associates, in chromosomally normal neonates, holoprosencephaly, severe facial dysmorphism, postaxial polydactyly and other congenital abnormalities, suggestive of trisomy 13." @default.