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Disease Ontology Browser
GM1 gangliosidosis type 2 (DOID:0080501)
Alliance: disease page
Synonyms: juvenile GM1 gangliosidosis
Alt IDs: OMIM:230600
Definition: A GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory