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- B85f6f40f018c3ecad4a64bbbeb9d93e3 hasDbXref "Orphanet:3033" @default.
- B85f6f40f018c3ecad4a64bbbeb9d93e3 type Axiom @default.
- B85f6f40f018c3ecad4a64bbbeb9d93e3 annotatedProperty IAO_0000115 @default.
- B85f6f40f018c3ecad4a64bbbeb9d93e3 annotatedSource MONDO_0017609 @default.
- B85f6f40f018c3ecad4a64bbbeb9d93e3 annotatedTarget "Renal tubular dysgenesis is a rare disorder of the fetus characterized by absent or poorly developed proximal tubules of the kidneys, persistent oligohydramnios, leading to Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia arthrogryposis and limb positioning defects), and skull ossification defects. It can be acquired during fetal development due to drugs taken by the mother or certain disorders (twin-twin transfusion syndrome, TTTS) or inherited in an autosomal recessive manner." @default.