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Metadata
ID DOID:0110791
Name hereditary spastic paraplegia 3A
Definition A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.
https://www.ncbi.nlm.nih.gov/pubmed/11685207
Xrefs

GARD:5041

ICD10CM:G11.4

OMIM:182600

ORDO:100984

Subsets

DO_rare_slim

Synonyms

autosomal dominant familial spastic paraplegia 1 [EXACT]

autosomal dominant spastic paraplegia 3 [EXACT]

autosomal dominant spastic paraplegia type 3 [EXACT]

FSP1 [EXACT]

SPG3A [EXACT]

strumpell disease [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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