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- B11ae9b98ff150d3f30d58d23a599e892 hasDbXref "Orphanet:3080" @default.
- B11ae9b98ff150d3f30d58d23a599e892 type Axiom @default.
- B11ae9b98ff150d3f30d58d23a599e892 annotatedProperty IAO_0000115 @default.
- B11ae9b98ff150d3f30d58d23a599e892 annotatedSource MONDO_0010203 @default.
- B11ae9b98ff150d3f30d58d23a599e892 annotatedTarget "Intellectual disability, Wolff type is a rare intellectual disability syndrome characterized by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias." @default.