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- B3e8ddbba7a006da85a2529796e4d6e51 hasDbXref "Orphanet:468661" @default.
- B3e8ddbba7a006da85a2529796e4d6e51 type Axiom @default.
- B3e8ddbba7a006da85a2529796e4d6e51 annotatedProperty IAO_0000115 @default.
- B3e8ddbba7a006da85a2529796e4d6e51 annotatedSource MONDO_0014644 @default.
- B3e8ddbba7a006da85a2529796e4d6e51 annotatedTarget "Autosomal recessive spastic paraplegia type 74 is a rare, genetic, spastic paraplegia-optic atrophy-neuropathy-related (SPOAN-like) disorder characterized by childhood onset of mild to moderate spastic paraparesis which manifests with gait impairment that very slowly progresses into late adulthood, hyperactive patellar reflex and bilateral extensor plantar response, in association with optic atrophy and typical symptoms of peripheral neuropathy, including reduced or absent ankle reflexes, lower limb atrophy and distal sensory impairment. Reduced visual acuity and pes cavus are frequently reported." @default.