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| Term | dilated cardiomyopathy 1P | ID (Ontology) | DOID:0110439 (Human Disease) |
| Definition | A dilated cardiomyopathy that has_material_basis_in mutation in the PLN gene on chromosome 6q22. | ||
| Also Known As | "CMD1P" | ||
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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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intrinsic cardiomyopathy |__dilated cardiomyopathy__ genetic disease | |__monogenic disease_______| dilated cardiomyopathy 1P 2 rec. |
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| Is a |
monogenic disease dilated cardiomyopathy |
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External Crossreferences & Linkouts
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ICD10CM:I42.0 MIM:609909 |
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