Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B10bd3418c2fccc22edc5f9564e6a2a64> ?p ?o ?g. }
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- B10bd3418c2fccc22edc5f9564e6a2a64 hasDbXref "GARD:0005355" @default.
- B10bd3418c2fccc22edc5f9564e6a2a64 type Axiom @default.
- B10bd3418c2fccc22edc5f9564e6a2a64 annotatedProperty IAO_0000115 @default.
- B10bd3418c2fccc22edc5f9564e6a2a64 annotatedSource MONDO_0016944 @default.
- B10bd3418c2fccc22edc5f9564e6a2a64 annotatedTarget "Chromosome 7p duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the short arm (p) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 7p duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Most cases are not inherited, but people can pass the duplication on to their children. Treatment is based on the signs and symptoms present in each person." @default.