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- B4fe5c5dc740ae6d587605cffd73ab6d9 hasDbXref "Orphanet:96063" @default.
- B4fe5c5dc740ae6d587605cffd73ab6d9 type Axiom @default.
- B4fe5c5dc740ae6d587605cffd73ab6d9 annotatedProperty IAO_0000115 @default.
- B4fe5c5dc740ae6d587605cffd73ab6d9 annotatedSource MONDO_0019868 @default.
- B4fe5c5dc740ae6d587605cffd73ab6d9 annotatedTarget "Mosaic trisomy 10 is a rare chromosomal anomaly syndrome, with a highly variable phenotype, principally characterized by growth delay, craniofacial dysmorphism (incl. prominent forehead, hypertelorism, upslanting palpebral fissures, blepharophimosis, low-set malformed large ears, high arched palate, cleft lip/palate, retrognathia) and cardiac, renal and skeletal (e.g. radial ray defects, scoliosis) malformations, with death usually ocurring neonatally or in early infancy. Other reported features include central nervous system and ear anomalies, as well as facial clefts and anal atresia." @default.