Rare familial disorder with hypertrophic cardiomyopathy
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Rare familial disorder with hypertrophic obstructive cardiomyopathy
Rare familial disorder with hypertrophic subaortic stenosis
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Number of Symptoms
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0
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OrphanetNr:
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99739
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OMIM Id:
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ICD-10:
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UMLs:
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C0949658
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MeSH:
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D024741
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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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Hypertrophic cardiomyopathy
-Rare cardiac disease
Rare genetic cardiac disease
-Rare genetic disease
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Comment:
| This term does not characterize a disease but a group of diseases. |
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |