Schindler disease Disease Ontology Browser

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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 the NAGA gene 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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