Visualize Submit Comment
Metadata
ID DOID:0110797
Name hereditary spastic paraplegia 45
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.
https://www.ncbi.nlm.nih.gov/pubmed/24482476
Xrefs

ICD10CM:G11.4

OMIM:613162

ORDO:320396

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 45 [EXACT]

autosomal recessive spastic paraplegia type 45 [EXACT]

autosomal recessive spastic paraplegia type 65 [EXACT]

SPG45 [EXACT]

SPG65 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

Add an item to the term tracker