Spastic paraplegia 89, autosomal recessive

Preferred Label : Spastic paraplegia 89, autosomal recessive;

Symbol : SPG89;

Type : Phenotype, molecular basis known;

Prefixed ID : #620379;

Details

Origin ID

620379;

UMLS CUI

C5830531;

Genes related to phenotype
- Autocrine motility factor receptor [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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