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Human Disease

hereditary spastic paraplegia 57

Term ID

DOID:0110809

Synonyms

autosomal recessive spastic paraplegia 57
autosomal recessive spastic paraplegia type 57
SPG57

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

References

ICD10CM:G11.4
MIM:615658
ORDO:431329

Ontology

Human Disease ( DOID:0110809 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models