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| Term | dilated cardiomyopathy 1X | ID (Ontology) | DOID:0110444 (Human Disease) |
| Definition | A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31. | ||
| Also Known As | "CMD1X" ; "dilated cardiomyopathy with mild or no proximal muscle weakness" | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease__ intrinsic cardiomyopathy | |__dilated cardiomyopathy_______| dilated cardiomyopathy 1X |
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| Is a |
autosomal recessive disease dilated cardiomyopathy |
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External Crossreferences & Linkouts
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ICD10CM:I42.0 MIM:611615 |
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