hereditary spastic paraplegia 43

Term ID

DOID:0110795

Synonyms

autosomal recessive spastic paraplegia 43
autosomal recessive spastic paraplegia type 43
SPG43

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12. https://www.ncbi.nlm.nih.gov/pubmed/23857908

References

ICD10CM:G11.4
MIM:615043
ORDO:320370

Ontology

Human Disease ( DOID:0110795 )

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