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| Term | Schindler disease type 3 | ID (Ontology) | DOID:0112320 (Human Disease) |
| Definition | A Schindler disease characterized by mild to moderate neurologic manifestations with onset after infancy but earlier than in Schindler disease type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the NAGA gene on chromosome 22q13.2. | ||
| Also Known As | "alpha-N-acetylgalactosaminidase deficiency type 3" ; "NAGA deficiency type 3" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ lysosomal storage disease____| Schindler disease |__Schindler disease type 3 |
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| Is a | Schindler disease | ||
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GARD:3903 ORDO:79281 |
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