hereditary spastic paraplegia 55

Term ID

DOID:0110807

Synonyms

autosomal recessive spastic paraplegia 55
autosomal recessive spastic paraplegia type 55
SPG55

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24. https://www.ncbi.nlm.nih.gov/pubmed/23188110

References

ICD10CM:G11.4
MIM:615035
ORDO:320375

Ontology

Human Disease ( DOID:0110807 )

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