Brugada syndrome 2
Brugada syndrome that has material basis in heterozygous mutation in the GPD1L gene on chromosome 3p22
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Brugada syndrome 2
Summary
Brugada syndrome 2 is a rare disease[1].
Key Facts
- Brugada syndrome 2's instance of is recorded as rare disease[2].
- Brugada syndrome 2's instance of is recorded as class of disease[3].
- Brugada syndrome 2's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 2's subclass of is recorded as monogenic disease[5].
- Brugada syndrome 2's MeSH descriptor ID is recorded as C567087[6].
- Brugada syndrome 2's OMIM ID is recorded as 611777[7].
- Brugada syndrome 2's Disease Ontology ID is recorded as DOID:0110219[8].
- Brugada syndrome 2's health specialty is recorded as cardiology[9].
- Brugada syndrome 2's genetic association is recorded as GPD1L[10].
- Brugada syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110219[11].
- Brugada syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0110219[12].
- Brugada syndrome 2's UMLS CUI is recorded as C2673193[13].
- Brugada syndrome 2's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Brugada syndrome 2's Mondo ID is recorded as MONDO_0012728[16].
- Brugada syndrome 2's UniProt disease ID is recorded as DI-00203[17].