Non-familial restrictive cardiomyopathy
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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0
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OrphanetNr:
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217720
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OMIM Id:
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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Restrictive cardiomyopathy
-Rare cardiac disease
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Comment:
| This term does not characterize a disease but a group of diseases. Annotations can be found at a more specific level. |
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |