Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5240f30c442ad9dd1f5fbac2b3bd25ab> ?p ?o ?g. }
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- B5240f30c442ad9dd1f5fbac2b3bd25ab hasDbXref "Orphanet:281" @default.
- B5240f30c442ad9dd1f5fbac2b3bd25ab type Axiom @default.
- B5240f30c442ad9dd1f5fbac2b3bd25ab annotatedProperty IAO_0000115 @default.
- B5240f30c442ad9dd1f5fbac2b3bd25ab annotatedSource MONDO_0007404 @default.
- B5240f30c442ad9dd1f5fbac2b3bd25ab annotatedTarget "Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism." @default.