Brugada syndrome 4
Brugada syndrome that has material basis in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12
Press Enter · cited answer in seconds
0 sources
Brugada syndrome 4
Summary
Brugada syndrome 4 is a rare disease[1].
Key Facts
- Brugada syndrome 4's instance of is recorded as rare disease[2].
- Brugada syndrome 4's instance of is recorded as class of disease[3].
- Brugada syndrome 4's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 4's subclass of is recorded as monogenic disease[5].
- Brugada syndrome 4's MeSH descriptor ID is recorded as C567508[6].
- Brugada syndrome 4's OMIM ID is recorded as 611876[7].
- Brugada syndrome 4's Disease Ontology ID is recorded as DOID:0110221[8].
- Brugada syndrome 4's health specialty is recorded as cardiology[9].
- Brugada syndrome 4's genetic association is recorded as CACNB2[10].
- Brugada syndrome 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110221[11].
- Brugada syndrome 4's exact match is recorded as http://identifiers.org/doid/DOID:0110221[12].
- Brugada syndrome 4's UMLS CUI is recorded as C2678477[13].
- Brugada syndrome 4's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 4's GARD rare disease ID is recorded as 10362[15].
- Brugada syndrome 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Brugada syndrome 4's Mondo ID is recorded as MONDO_0012743[17].
- Brugada syndrome 4's UniProt disease ID is recorded as DI-00205[18].