Spastic paraplegia 79a, autosomal dominant, with ataxia

Preferred Label : Spastic paraplegia 79a, autosomal dominant, with ataxia;

Symbol : SPG79A;

Type : Phenotype, molecular basis known;

Prefixed ID : #620221;

Details

Origin ID

620221;

UMLS CUI

C5774300;

Genes related to phenotype
- Ubiquitin carboxyl-terminal esterase l1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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