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- B392ef8c3a2251cd8afa03d86dc989e93 hasDbXref "NCIT:P378" @default.
- B392ef8c3a2251cd8afa03d86dc989e93 type Axiom @default.
- B392ef8c3a2251cd8afa03d86dc989e93 annotatedProperty IAO_0000115 @default.
- B392ef8c3a2251cd8afa03d86dc989e93 annotatedSource MONDO_0008564 @default.
- B392ef8c3a2251cd8afa03d86dc989e93 annotatedTarget "A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. DiGeorge syndrome is associated with abnormalities of chromosome 22. Also known as DiGeorge anomaly." @default.