Brugada syndrome 8
Brugada syndrome that has material basis in heterozygous mutation in the HCN4 gene on chromosome 15q24
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Brugada syndrome 8
Summary
Brugada syndrome 8 is a rare disease[1].
Key Facts
- Brugada syndrome 8's instance of is recorded as rare disease[2].
- Brugada syndrome 8's instance of is recorded as class of disease[3].
- Brugada syndrome 8's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 8's subclass of is recorded as monogenic disease[5].
- Brugada syndrome 8's MeSH descriptor ID is recorded as C567732[6].
- Brugada syndrome 8's OMIM ID is recorded as 613123[7].
- Brugada syndrome 8's Disease Ontology ID is recorded as DOID:0110225[8].
- Brugada syndrome 8's health specialty is recorded as cardiology[9].
- Brugada syndrome 8's genetic association is recorded as HCN4[10].
- Brugada syndrome 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110225[11].
- Brugada syndrome 8's exact match is recorded as http://identifiers.org/doid/DOID:0110225[12].
- Brugada syndrome 8's UMLS CUI is recorded as C2751083[13].
- Brugada syndrome 8's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Brugada syndrome 8's Mondo ID is recorded as MONDO_0013148[16].
- Brugada syndrome 8's UniProt disease ID is recorded as DI-02557[17].