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- B1f75ea95be638fdcdb63d13fcbac19bf hasDbXref "Orphanet:2821" @default.
- B1f75ea95be638fdcdb63d13fcbac19bf type Axiom @default.
- B1f75ea95be638fdcdb63d13fcbac19bf annotatedProperty IAO_0000115 @default.
- B1f75ea95be638fdcdb63d13fcbac19bf annotatedSource MONDO_0008442 @default.
- B1f75ea95be638fdcdb63d13fcbac19bf annotatedTarget "Spastic paraplegia-neuropathy-poikiloderma syndrome is a complex form of hereditary spastic paraplegia characterized by spastic paraplegia, demyelinating peripheral sensorimotor neuropathy, poikiloderma (manifesting with loss of eyebrows and eyelashes in childhood in addition to delicate, smooth, and wasted skin) and distal amyotrophy (presenting after puberty). There have been no further descriptions in the literature since 1992." @default.