hereditary spastic paraplegia 62

Term ID

DOID:0110813

Synonyms

autosomal recessive spastic paraplegia 62
autosomal recessive spastic paraplegia type 62
SPG62

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

ICD10CM:G11.4
MIM:615681
ORDO:401785

Ontology

Human Disease ( DOID:0110813 )

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