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- B29db6ea30a0d9ac19d7e4984ecee038b hasDbXref "GARD:0001340" @default.
- B29db6ea30a0d9ac19d7e4984ecee038b type Axiom @default.
- B29db6ea30a0d9ac19d7e4984ecee038b annotatedProperty IAO_0000115 @default.
- B29db6ea30a0d9ac19d7e4984ecee038b annotatedSource MONDO_0016903 @default.
- B29db6ea30a0d9ac19d7e4984ecee038b annotatedTarget "Chromosome 4q deletion is a chromosome abnormality that affects many different parts of the body. People with this condition are missing genetic material located on the long arm (q) of chromosome 4 in each cell. The severity of the condition and the associated signs and symptoms vary based on the size and location of the deletion and which genes are involved. Common features shared by many people with this deletion includedistinctive craniofacial features, skeletal abnormalities, heart defects, intellectual disability, developmental delay, and short stature. Most cases are not inherited, although affectedpeople can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person." @default.