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Disease Ontology Browser
Schindler disease (DOID:0112317)
Alliance: disease page
Synonyms: 'alpha-N-acetylgalactosaminidase deficiency'; 'NAGA deficiency'
Alt IDs: ORDO:3137
Definition: A lysosomal storage disease that has_material_basis_in homozygous or compound heterozygous mutation in NAGA on chromosome 22q13.2.


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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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory