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Metadata
ID DOID:0110809
Name hereditary spastic paraplegia 57
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12.
https://www.ncbi.nlm.nih.gov/pubmed/23479643
Xrefs

ICD10CM:G11.4

OMIM:615658

ORDO:431329

Synonyms

autosomal recessive spastic paraplegia 57 [EXACT]

autosomal recessive spastic paraplegia type 57 [EXACT]

SPG57 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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