hereditary spastic paraplegia 61

Term ID

DOID:0110812

Synonyms

autosomal recessive spastic paraplegia 61
autosomal recessive spastic paraplegia type 61
SPG61

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

ICD10CM:G11.4
MIM:615685
ORDO:401780

Ontology

Human Disease ( DOID:0110812 )

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