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hereditary spastic paraplegia 3A | RareConnect | RareConnect.io

/hereditary spastic paraplegia

/hereditary spastic paraplegia 3A

hereditary spastic paraplegia 3A

Rare Disease

MONDO:0008437

Also Known As

ATL1 hereditary spastic paraplegiaFSP1SPG3AStrümpell diseaseautosomal dominant familial spastic paraplegia 1autosomal dominant spastic paraplegia 3autosomal dominant spastic paraplegia type 3hereditary spastic paraplegia caused by mutation in ATL1hereditary spastic paraplegia type 3Aspastic Paraplegia 3Aspastic paraplegia 3a, autosomal dominantstrumpell diseaseSpg3Strumpell diseasefamilial spastic paraplegia, autosomal dominant, 1spastic paraplegia 3spastic paraplegia 3, autosomal dominant

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:182600 ↗

Orphanet

Orphanet:100984 ↗

GARD

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