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Metadata
ID DOID:0110773
Name hereditary spastic paraplegia 2
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.
https://www.ncbi.nlm.nih.gov/pubmed/8012387
Xrefs

GARD:4923

ICD10CM:G11.4

OMIM:312920

ORDO:99015

Subsets

DO_rare_slim

Synonyms

spastic paraplegia type 2 [EXACT]

SPG2 [EXACT]

X-linked spastic paraplegia 2 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a X-linked recessive disease

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