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- B633270c40a6250506ba6c2510a25e52c hasDbXref "Orphanet:96063" @default.
- B633270c40a6250506ba6c2510a25e52c type Axiom @default.
- B633270c40a6250506ba6c2510a25e52c annotatedProperty IAO_0000115 @default.
- B633270c40a6250506ba6c2510a25e52c annotatedSource MONDO_0019868 @default.
- B633270c40a6250506ba6c2510a25e52c 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.