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- B693ee32c48f8ae2adf057bcfe20fe3ec hasDbXref "Orphanet:171612" @default.
- B693ee32c48f8ae2adf057bcfe20fe3ec type Axiom @default.
- B693ee32c48f8ae2adf057bcfe20fe3ec annotatedProperty IAO_0000115 @default.
- B693ee32c48f8ae2adf057bcfe20fe3ec annotatedSource MONDO_0012766 @default.
- B693ee32c48f8ae2adf057bcfe20fe3ec annotatedTarget "Autosomal dominant spastic paraplegia type 37 is a pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients." @default.