Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

LONG QT SYNDROME 3

Synonyms

LQT3/6, DIGENIC

ID

http://purl.bioontology.org/ontology/OMIM/603830

altLabel

LQT3/6, DIGENIC

LONG QT SYNDROME 2/3, DIGENIC

LONG QT SYNDROME 3/6, DIGENIC

LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO

LQT3

LQT2/3, DIGENIC

cui

C3276241

C3276240

C1859062

C1838527

Gene Locus

3p21

Gene Symbol

CDCD2

CMD1E

SCN5A

HB1

SSS1

LQT3

VF1

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU005010

http://purl.bioontology.org/ontology/OMIM/MTHU029137

http://purl.bioontology.org/ontology/OMIM/MTHU029359

http://purl.bioontology.org/ontology/OMIM/MTHU005008

http://purl.bioontology.org/ontology/OMIM/MTHU005016

http://purl.bioontology.org/ontology/OMIM/MTHU005014

http://purl.bioontology.org/ontology/OMIM/MTHU005011

http://purl.bioontology.org/ontology/OMIM/MTHU005012

http://purl.bioontology.org/ontology/OMIM/MTHU005009

http://purl.bioontology.org/ontology/OMIM/MTHU005017

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

603830

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

LONG QT SYNDROME 3

tui

T033

T047

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http://purl.bioontology.org/ontology/MESH/C565840 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C565840 Medical Subject Headings LOOM
http://purl.obolibrary.org/obo/DOID_0110646 Human Disease Ontology 123 LOOM