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Metadata
ID DOID:0110793
Name hereditary spastic paraplegia 41
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.
https://www.ncbi.nlm.nih.gov/pubmed/18364116
Xrefs

ICD10CM:G11.4

OMIM:613364

ORDO:320355

Synonyms

autosomal dominant spastic paraplegia 41 [EXACT]

autosomal dominant spastic paraplegia type 41 [EXACT]

SPG41 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

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