hereditary spastic paraplegia 56

Term ID

DOID:0110808

Synonyms

autosomal recessive spastic paraplegia 56
autosomal recessive spastic paraplegia type 56
SPG56

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23176821

References

ICD10CM:G11.4
MIM:615030
ORDO:320411

Ontology

Human Disease ( DOID:0110808 )

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