Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B91410eaac729a81e1e0ae6ece333c085> ?p ?o ?g. }
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- B91410eaac729a81e1e0ae6ece333c085 hasDbXref "Orphanet:1358" @default.
- B91410eaac729a81e1e0ae6ece333c085 type Axiom @default.
- B91410eaac729a81e1e0ae6ece333c085 annotatedProperty IAO_0000115 @default.
- B91410eaac729a81e1e0ae6ece333c085 annotatedSource MONDO_0800437 @default.
- B91410eaac729a81e1e0ae6ece333c085 annotatedTarget "A rare condition characterized by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay." @default.