Brugada syndrome 5
Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13
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Brugada syndrome 5
Summary
Brugada syndrome 5 is a rare disease[1].
Key Facts
- Brugada syndrome 5's instance of is recorded as rare disease[2].
- Brugada syndrome 5's instance of is recorded as class of disease[3].
- Brugada syndrome 5's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 5's subclass of is recorded as monogenic disease[5].
- Brugada syndrome 5's OMIM ID is recorded as 612838[6].
- Brugada syndrome 5's Disease Ontology ID is recorded as DOID:0110222[7].
- Brugada syndrome 5's health specialty is recorded as cardiology[8].
- Brugada syndrome 5's genetic association is recorded as SCN1B[9].
- Brugada syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110222[10].
- Brugada syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0110222[11].
- Brugada syndrome 5's UMLS CUI is recorded as C2748541[12].
- Brugada syndrome 5's UMLS CUI is recorded as C2748542[13].
- Brugada syndrome 5's ICD-10-CM is recorded as I49.8[14].
- Brugada syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Brugada syndrome 5's Mondo ID is recorded as MONDO_0013015[16].
- Brugada syndrome 5's UniProt disease ID is recorded as DI-02502[17].