Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bee687820805053f63f7e76e69a16e84f> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bee687820805053f63f7e76e69a16e84f hasDbXref "GARD:0003760" @default.
- Bee687820805053f63f7e76e69a16e84f type Axiom @default.
- Bee687820805053f63f7e76e69a16e84f annotatedProperty IAO_0000115 @default.
- Bee687820805053f63f7e76e69a16e84f annotatedSource MONDO_0016905 @default.
- Bee687820805053f63f7e76e69a16e84f annotatedTarget "Chromosome 6q 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 6. 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 6q deletion include developmental delay, intellectual disability, 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.