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| Term | autosomal recessive centronuclear myopathy | ID (Ontology) | DOID:0111216 (Human Disease) |
| Definition | A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. | ||
| Also Known As | "AR-CNM" | ||
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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 genetic disease |__autosomal recessive disease__ congenital structural myopathy | |__centronuclear myopathy_______| autosomal recessive centronuclear myopathy 7 rec. |__centronuclear myopathy 2 4 rec. |__centronuclear myopathy 5 1 rec. |__centronuclear myopathy 6 with fiber-type disproportion 2 rec. |
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| Is a |
autosomal recessive disease centronuclear myopathy |
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GARD:12718 ORDO:169186 |
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