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- B5f14bea93b416678792c7d0d871f61e6 hasDbXref "Orphanet:397695" @default.
- B5f14bea93b416678792c7d0d871f61e6 type Axiom @default.
- B5f14bea93b416678792c7d0d871f61e6 annotatedProperty IAO_0000115 @default.
- B5f14bea93b416678792c7d0d871f61e6 annotatedSource MONDO_0018341 @default.
- B5f14bea93b416678792c7d0d871f61e6 annotatedTarget "A rare chromosomal anomaly syndrome, resulting from the partial deletion of the long arm of chromosome 3, characterized by mild to severe intellectual disability, neuropsychiatric disorders of the psychotic and dysthymic spectrum, mild distinctive facial dysmorphism (incl. slender face, deep-set eyes, high nasal bridge with a hooked nose, small, low- set ears, short philtrum, small mouth with thin upper lip, prognathism) and a marfanoid habitus." @default.