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- B9ef21c7ff40f67a740a5d78d6ed36ca4 hasDbXref "Orphanet:2769" @default.
- B9ef21c7ff40f67a740a5d78d6ed36ca4 type Axiom @default.
- B9ef21c7ff40f67a740a5d78d6ed36ca4 annotatedProperty IAO_0000115 @default.
- B9ef21c7ff40f67a740a5d78d6ed36ca4 annotatedSource MONDO_0009801 @default.
- B9ef21c7ff40f67a740a5d78d6ed36ca4 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.