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| Term | infantile onset multisystem autoimmune disease 2 | ID (Ontology) | DOID:0061161 (Human Disease) |
| Definition | An infantile onset multisystem autoimmune disease that has_material_basis_in compound heterozygous mutation in the ZAP70 gene on chromosome 2q12. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease_____________________ autoimmune disease | |__infantile onset multisystem autoimmune disease__| infantile onset multisystem autoimmune disease 2 1 rec. |
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| Is a |
autosomal recessive disease infantile onset multisystem autoimmune disease |
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External Crossreferences & Linkouts
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| MIM:617006 | |||