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Human Disease

hereditary spastic paraplegia 32

Term ID

DOID:0110783

Synonyms

autosomal recessive spastic paraplegia 32
autosomal recessive spastic paraplegia type 32
SPG32

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

References

GARD:12749
ICD10CM:G11.4
MIM:611252
ORDO:171622

Ontology

Human Disease ( DOID:0110783 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models