Brugada syndrome 3
Brugada syndrome that has material basis in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13
Press Enter · cited answer in seconds
0 sources
Brugada syndrome 3
Summary
Brugada syndrome 3 is a rare disease[1].
Key Facts
- Brugada syndrome 3's instance of is recorded as rare disease[2].
- Brugada syndrome 3's instance of is recorded as class of disease[3].
- Brugada syndrome 3's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 3's subclass of is recorded as monogenic disease[5].
- Brugada syndrome 3's MeSH descriptor ID is recorded as C567509[6].
- Brugada syndrome 3's OMIM ID is recorded as 611875[7].
- Brugada syndrome 3's Disease Ontology ID is recorded as DOID:0110220[8].
- Brugada syndrome 3's health specialty is recorded as cardiology[9].
- Brugada syndrome 3's genetic association is recorded as CACNA1C[10].
- Brugada syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110220[11].
- Brugada syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0110220[12].
- Brugada syndrome 3's UMLS CUI is recorded as C2678478[13].
- Brugada syndrome 3's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 3's GARD rare disease ID is recorded as 10361[15].
- Brugada syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Brugada syndrome 3's Mondo ID is recorded as MONDO_0012742[17].
- Brugada syndrome 3's UniProt disease ID is recorded as DI-00204[18].