Brugada syndrome 1
Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22
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Brugada syndrome 1
Summary
Brugada syndrome 1 is a class of disease[1].
Key Facts
- Brugada syndrome 1's instance of is recorded as class of disease[2].
- Brugada syndrome 1's subclass of is recorded as Brugada syndrome[3].
- Brugada syndrome 1's subclass of is recorded as autosomal dominant disease[4].
- Brugada syndrome 1's OMIM ID is recorded as 601144[5].
- Brugada syndrome 1's Disease Ontology ID is recorded as DOID:0110218[6].
- Brugada syndrome 1's health specialty is recorded as cardiology[7].
- Brugada syndrome 1's genetic association is recorded as SCN5A[8].
- Brugada syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110218[9].
- Brugada syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:0110218[10].
- Brugada syndrome 1's UMLS CUI is recorded as CN029323[11].
- Brugada syndrome 1's UMLS CUI is recorded as C1142166[12].
- Brugada syndrome 1's UMLS CUI is recorded as C2748542[13].
- Brugada syndrome 1's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Brugada syndrome 1's Mondo ID is recorded as MONDO_0011001[16].
- Brugada syndrome 1's UniProt disease ID is recorded as DI-00202[17].