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- Be84dd625fe26c13e76a88f09b6a593dc hasDbXref "GARD:0003744" @default.
- Be84dd625fe26c13e76a88f09b6a593dc type Axiom @default.
- Be84dd625fe26c13e76a88f09b6a593dc annotatedProperty IAO_0000115 @default.
- Be84dd625fe26c13e76a88f09b6a593dc annotatedSource MONDO_0016901 @default.
- Be84dd625fe26c13e76a88f09b6a593dc annotatedTarget "Chromosome 2q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 2. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 2q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person." @default.