Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

BRUGADA SYNDROME 5
Synonyms

CARDIAC CONDUCTION DEFECT, NONSPECIFIC
ID

http://purl.bioontology.org/ontology/OMIM/612838
altLabel

CARDIAC CONDUCTION DEFECT, NONSPECIFIC

BRGDA5
cui

C2748542

C2748541
Gene Locus

19q13.1
Gene Symbol

GEFSP1

EIEE52

ATFB13

BRGDA5

SCN1B
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

612838
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

BRUGADA SYNDROME 5
tui

T047
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http://purl.bioontology.org/ontology/MESH/C567557 Medical Subject Headings CUI
http://purl.obolibrary.org/obo/DOID_0110222 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/MESH/C567556 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C567556 Medical Subject Headings LOOM