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Metadata
ID DOID:0110782
Name hereditary spastic paraplegia 31
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.
https://www.ncbi.nlm.nih.gov/pubmed/16826527
Xrefs

GARD:10817

ICD10CM:G11.4

OMIM:610250

ORDO:101011

Synonyms

autosomal dominant spastic paraplegia 31 [EXACT]

autosomal dominant spastic paraplegia type 31 [EXACT]

SPG31 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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