Brugada syndrome 7
Brugada syndrome that has material basis in heterozygous mutation in the SCN3B gene on chromosome 11q24
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Brugada syndrome 7
Summary
Brugada syndrome 7 is a class of disease[1].
Key Facts
- Brugada syndrome 7's instance of is recorded as class of disease[2].
- Brugada syndrome 7's subclass of is recorded as Brugada syndrome[3].
- Brugada syndrome 7's subclass of is recorded as autosomal dominant disease[4].
- Brugada syndrome 7's MeSH descriptor ID is recorded as C567734[5].
- Brugada syndrome 7's OMIM ID is recorded as 613120[6].
- Brugada syndrome 7's Disease Ontology ID is recorded as DOID:0110224[7].
- Brugada syndrome 7's health specialty is recorded as cardiology[8].
- Brugada syndrome 7's genetic association is recorded as SCN3B[9].
- Brugada syndrome 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110224[10].
- Brugada syndrome 7's exact match is recorded as http://identifiers.org/doid/DOID:0110224[11].
- Brugada syndrome 7's UMLS CUI is recorded as C2751088[12].
- Brugada syndrome 7's ICD-10-CM is recorded as I49.8[13].
- Brugada syndrome 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Brugada syndrome 7's Mondo ID is recorded as MONDO_0013146[15].
- Brugada syndrome 7's UniProt disease ID is recorded as DI-02503[16].