/autosomal recessive spastic paraplegia type 78

autosomal recessive spastic paraplegia type 78

Rare Disease

MONDO:0014975

Also Known As

ATP13A2 hereditary spastic paraplegiaSPG78hereditary spastic paraplegia caused by mutation in ATP13A2spastic paraplegia 78, autosomal recessivespastic paraplegia 78, autosomal recessive; SPG78

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.

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Comprehensive, easy-to-understand information about this condition

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Associated Genes

ATP13A2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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autosomal recessive spastic paraplegia type 78

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases