hereditary spastic paraplegia 77

Term ID

DOID:0110822

Synonyms

autosomal recessive spastic paraplegia 77
SPG77

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/26553276

References

ICD10CM:G11.4
OMIM:617046
ORDO:466722

Ontology

Human Disease ( DOID:0110822 )

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

Citations