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Metadata
ID DOID:0110820
Name hereditary spastic paraplegia 75
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.
https://www.ncbi.nlm.nih.gov/pubmed/24482476
Xrefs

ICD10CM:G11.4

OMIM:616680

ORDO:459056

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 75 [EXACT]

autosomal recessive spastic paraplegia type 75 [EXACT]

SPG75 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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