arrhythmogenic right ventricular dysplasia 2
arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the cardiac ryanodine receptor-2 gene (RYR2) on chromosome 1q43
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arrhythmogenic right ventricular dysplasia 2
Summary
arrhythmogenic right ventricular dysplasia 2 is a rare disease[1].
Key Facts
- arrhythmogenic right ventricular dysplasia 2's instance of is recorded as rare disease[2].
- arrhythmogenic right ventricular dysplasia 2's instance of is recorded as class of disease[3].
- arrhythmogenic right ventricular dysplasia 2's subclass of is recorded as arrhythmogenic right ventricular cardiomyopathy[4].
- arrhythmogenic right ventricular dysplasia 2's subclass of is recorded as autosomal dominant disease[5].
- arrhythmogenic right ventricular dysplasia 2's MeSH descriptor ID is recorded as C563409[6].
- arrhythmogenic right ventricular dysplasia 2's OMIM ID is recorded as 600996[7].
- arrhythmogenic right ventricular dysplasia 2's Disease Ontology ID is recorded as DOID:0110071[8].
- arrhythmogenic right ventricular dysplasia 2's health specialty is recorded as cardiology[9].
- arrhythmogenic right ventricular dysplasia 2's genetic association is recorded as RYR2[10].
- arrhythmogenic right ventricular dysplasia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110071[11].
- arrhythmogenic right ventricular dysplasia 2's exact match is recorded as http://identifiers.org/doid/DOID:0110071[12].
- arrhythmogenic right ventricular dysplasia 2's UMLS CUI is recorded as C1832931[13].
- arrhythmogenic right ventricular dysplasia 2's ICD-10-CM is recorded as I42.8[14].
- arrhythmogenic right ventricular dysplasia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- arrhythmogenic right ventricular dysplasia 2's Mondo ID is recorded as MONDO_0010975[16].