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| Term | mitochondrial DNA depletion syndrome 19 | ID (Ontology) | DOID:0070450 (Human Disease) |
| Definition | A mitochondrial DNA depletion syndrome that has_material_basis_in compound heterozygous mutation in the SLC25A10 gene on chromosome 17q25.3. | ||
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| DO.org | |||
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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___________ mitochondrial metabolism disease | |__mitochondrial DNA depletion syndrome__| mitochondrial DNA depletion syndrome 19 6 rec. |
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| Is a |
autosomal recessive disease mitochondrial DNA depletion syndrome |
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External Crossreferences & Linkouts
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| MIM:618972 | |||