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- Bd833ef5cca11bf71001aac795d73de52 hasDbXref "GARD:0003744" @default.
- Bd833ef5cca11bf71001aac795d73de52 type Axiom @default.
- Bd833ef5cca11bf71001aac795d73de52 annotatedProperty IAO_0000115 @default.
- Bd833ef5cca11bf71001aac795d73de52 annotatedSource MONDO_0016901 @default.
- Bd833ef5cca11bf71001aac795d73de52 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.