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- Bd1baad78d213b14ed08319e4b6a5af4e hasDbXref "OMIM:617537" @default.
- Bd1baad78d213b14ed08319e4b6a5af4e type Axiom @default.
- Bd1baad78d213b14ed08319e4b6a5af4e annotatedProperty IAO_0000115 @default.
- Bd1baad78d213b14ed08319e4b6a5af4e annotatedSource MONDO_0044323 @default.
- Bd1baad78d213b14ed08319e4b6a5af4e annotatedTarget "Rahman syndrome is characterized by mild to severe intellectual disability associated with variable somatic overgrowth manifest as increased birth length, height, weight, and/or head circumference. The overgrowth is apparent in infancy and may lessen with time or persist. The phenotype is highly variable; some individuals may have other minor anomalies, including dysmorphic facial features, strabismus, or camptodactyly. The disorder is thought to result from a defect in epigenetic regulation (summary by {1:Tatton-Brown et al., 2017})." @default.