Search Ontology:
Human Disease
Brugada syndrome 2
- Term ID
- DOID:0110219
- Synonyms
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- BRGDA2
- Definition
- A Brugada syndrome that has_material_basis_in heterozygous mutation in the GPD1L gene on chromosome 3p22. https://www.ncbi.nlm.nih.gov/pubmed/17967977
- References
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- ICD10CM:I49.8
- MESH:C567087
- MIM:611777
- Ontology
- Human Disease ( DOID:0110219 )
- is a type of
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Genes Involved
Zebrafish Models