Spastic paraplegia 18a, autosomal dominant

Preferred Label : Spastic paraplegia 18a, autosomal dominant;

Symbol : SPG18A;

Type : Phenotype, molecular basis known;

Prefixed ID : #620512;

Details

Origin ID

620512;

UMLS CUI

C5882694;

Genes related to phenotype
- Endoplasmic reticulum lipid raft-associated protein 2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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