" /> Spastic paraplegia 31, autosomal dominant - CISMeF





Preferred Label : Spastic paraplegia 31, autosomal dominant;

Symbol : SPG31;

CISMeF acronym : SPG31;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the receptor expression-enhancing protein-1 gene (REEP1, 609139.0001);

Prefixed ID : #610250;

Details


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02/05/2025


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