Brugada syndrome 9
Brugada syndrome that has material basis in heterozygous mutation in the KCND3 gene on chromosome 1p13
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Brugada syndrome 9
Summary
Brugada syndrome 9 is a rare disease[1].
Key Facts
- Brugada syndrome 9's instance of is recorded as rare disease[2].
- Brugada syndrome 9's instance of is recorded as class of disease[3].
- Brugada syndrome 9's subclass of is recorded as Brugada syndrome[4].
- Brugada syndrome 9's subclass of is recorded as autosomal dominant disease[5].
- Brugada syndrome 9's OMIM ID is recorded as 616399[6].
- Brugada syndrome 9's Disease Ontology ID is recorded as DOID:0110226[7].
- Brugada syndrome 9's health specialty is recorded as cardiology[8].
- Brugada syndrome 9's genetic association is recorded as KCND3[9].
- Brugada syndrome 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110226[10].
- Brugada syndrome 9's exact match is recorded as http://identifiers.org/doid/DOID:0110226[11].
- Brugada syndrome 9's UMLS CUI is recorded as C4225340[12].
- Brugada syndrome 9's ICD-10-CM is recorded as I49.8[13].
- Brugada syndrome 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Brugada syndrome 9's Mondo ID is recorded as MONDO_0014621[15].
- Brugada syndrome 9's UniProt disease ID is recorded as DI-04444[16].