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Metadata
ID DOID:0110794
Name hereditary spastic paraplegia 42
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.
https://www.ncbi.nlm.nih.gov/pubmed/19061983
Xrefs

ICD10CM:G11.4

OMIM:612539

ORDO:171863

Synonyms

autosomal dominant spastic paraplegia 42 [EXACT]

autosomal dominant spastic paraplegia type 42 [EXACT]

SPG42 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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