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- B40734748a53e9c6e3d3cb8d0b17b88fc hasDbXref "OMIM:617450" @default.
- B40734748a53e9c6e3d3cb8d0b17b88fc type Axiom @default.
- B40734748a53e9c6e3d3cb8d0b17b88fc annotatedProperty IAO_0000115 @default.
- B40734748a53e9c6e3d3cb8d0b17b88fc annotatedSource MONDO_0044318 @default.
- B40734748a53e9c6e3d3cb8d0b17b88fc annotatedTarget "IDDGIP is an autosomal dominant syndromic neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability with speech delay, and behavioral abnormalities. Most patients have variable additional features, including feeding and gastrointestinal difficulties, high pain threshold and/or hypersensitivity to sound, and dysmorphic features, including mild facial abnormalities, strabismus, and small hands and feet (summary by {1:Jansen et al., 2017})." @default.