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Metadata
ID DOID:0110783
Name hereditary spastic paraplegia 32
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.
https://www.ncbi.nlm.nih.gov/pubmed/17515546
Xrefs

GARD:12749

ICD10CM:G11.4

OMIM:611252

ORDO:171622

Synonyms

autosomal recessive spastic paraplegia 32 [EXACT]

autosomal recessive spastic paraplegia type 32 [EXACT]

SPG32 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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