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
• OMIM:615658
• ORDO:431329

Ontology

Human Disease   ( DOID:0110809 )