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Metadata
ID DOID:0110813
Name hereditary spastic paraplegia 62
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.
https://www.ncbi.nlm.nih.gov/pubmed/24482476
Xrefs

ICD10CM:G11.4

MIM:615681

ORDO:401785

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 62 [EXACT]

autosomal recessive spastic paraplegia type 62 [EXACT]

SPG62 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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