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Human Disease and Mouse Model Detail
Human Disease

Term: Spastic Paraplegia 9, Autosomal Dominant; SPG9
OMIM ID: 601162

Synonyms Cataracts with Motor Neuronopathy, Short Stature, and Skeletal Abnormalities; Spastic Paraparesis with Amyopathy, Cataracts, and Gastroesophageal Reflux
Associated Genes
 There are currently no human or mouse genes associated with this disease in the MGI database.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory