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- Bc82b4bcb9da944f09a01d0f64d299770 hasDbXref "Orphanet:85292" @default.
- Bc82b4bcb9da944f09a01d0f64d299770 type Axiom @default.
- Bc82b4bcb9da944f09a01d0f64d299770 annotatedProperty IAO_0000115 @default.
- Bc82b4bcb9da944f09a01d0f64d299770 annotatedSource MONDO_0010534 @default.
- Bc82b4bcb9da944f09a01d0f64d299770 annotatedTarget "Spinocerebellar ataxia, X-linked, type 4 is characterized by ataxia, pyramidal tract signs and adult-onset dementia. It has been described in three generations of one large family. The disease manifests during early childhood with delayed walking and tremor. The pyramidal signs appear progressively and by adulthood memory problems and dementia gradually become apparent. Transmission is X-linked but the causative gene has not yet been identified. The disease is usually fatal during the sixth decade of life." @default.