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Metadata
ID DOID:0110787
Name hereditary spastic paraplegia 36
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.
https://www.ncbi.nlm.nih.gov/pubmed/19357379
Xrefs

ICD10CM:G11.4

OMIM:613096

ORDO:320365

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 36 [EXACT]

autosomal dominant spastic paraplegia type 36 [EXACT]

SPG36 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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