Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia

Preferred Label : Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia;

Symbol : SPG91;

Type : Phenotype, molecular basis known;

Prefixed ID : #620538;

Details

Origin ID

620538;

UMLS CUI

C5882701;

Genes related to phenotype
- Spectrin, alpha, nonerythrocytic 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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