About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 61 (DOID:0110812)
Synonyms: autosomal recessive spastic paraplegia 61; autosomal recessive spastic paraplegia type 61; SPG61
Alt IDs: OMIM:615685, ICD10CM:G11.4, ORDO:401780
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
07/11/2017
MGI 6.10
The Jackson Laboratory