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- B12cd58de18bacb859f07fed484a9665f hasDbXref "Orphanet:2769" @default.
- B12cd58de18bacb859f07fed484a9665f type Axiom @default.
- B12cd58de18bacb859f07fed484a9665f annotatedProperty IAO_0000115 @default.
- B12cd58de18bacb859f07fed484a9665f annotatedSource MONDO_0009801 @default.
- B12cd58de18bacb859f07fed484a9665f annotatedTarget "Familial osteodysplasia, Anderson type is a rare, genetic dysostosis disorder characterized by craniofacial bone abnormalities (i.e. midface hypoplasia, broad, flat nasal bridge, narrow, thin prognathic mandible with pointed chin, malocclusion, partial dental agenesis) associated with additional osseous anomalies, including scoliosis, calvarial thinning, pointed spinous processes, clinodactyly and abnormal phalanges. Elevated erythrocyte sedimentation rate, hyperuricemia and hypertension have also been reported. There have been no further descriptions in the literature since 1982." @default.