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- B9557dcb93eab6b09bdb687030f283b9f hasDbXref "Orphanet:8" @default.
- B9557dcb93eab6b09bdb687030f283b9f type Axiom @default.
- B9557dcb93eab6b09bdb687030f283b9f annotatedProperty IAO_0000115 @default.
- B9557dcb93eab6b09bdb687030f283b9f annotatedSource MONDO_0019339 @default.
- B9557dcb93eab6b09bdb687030f283b9f annotatedTarget "47, XYY syndrome is a sex chromosome aneuploidy where males receive an additional Y chromosome, and is characterized clinically by tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder." @default.