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Metadata
ID DOID:0110807
Name hereditary spastic paraplegia 55
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24.
https://www.ncbi.nlm.nih.gov/pubmed/23188110
Xrefs

ICD10CM:G11.4

OMIM:615035

ORDO:320375

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 55 [EXACT]

autosomal recessive spastic paraplegia type 55 [EXACT]

SPG55 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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