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Metadata
ID DOID:0110814
Name hereditary spastic paraplegia 63
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.
https://www.ncbi.nlm.nih.gov/pubmed/24482476
Xrefs

ICD10CM:G11.4

MIM:615686

ORDO:401805

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 63 [EXACT]

spastic paraplegia 63 [EXACT]

SPG63 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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