Sudden death - OMIM - NCBI

Sudden death - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Sudden death" 

%212130 - CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH

OMIM:

 

212130

Gene summaries Genetic tests Medical literature

Select item 1150802.

#115080 - CARDIAC CONDUCTION DEFECT

SUDDEN CARDIAC DEATH, INCLUDED; SCD, INCLUDED

Cytogenetic locations: 17p11.2

OMIM:

 

115080

Gene summaries Genetic tests Medical literature

Select item 6088003.

#608800 - SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME; SIDDT

Cytogenetic locations: 6q22.1

OMIM:

 

608800

Gene summaries Genetic tests Medical literature

Select item 2204004.

#220400 - JERVELL AND LANGE-NIELSEN SYNDROME 1; JLNS1

Cytogenetic locations: 11p15.5-p15.4

OMIM:

 

220400

Gene summaries Genetic tests Medical literature

Select item 6011445.

#601144 - BRUGADA SYNDROME 1; BRGDA1

CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED

Cytogenetic locations: 3p22.2

OMIM:

 

601144

Gene summaries Genetic tests Medical literature

Select item 2721206.

#272120 - SUDDEN INFANT DEATH SYNDROME

Cytogenetic locations: 3p22.2

OMIM:

 

272120

Gene summaries Genetic tests Medical literature

Select item 2724307.

#272430 - COLD-INDUCED SWEATING SYNDROME 1; CISS1

Cytogenetic locations: 19p13.11

OMIM:

 

272430

Gene summaries Genetic tests Medical literature

Select item 6172238.

#617223 - SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED; SCFAI

Cytogenetic locations: 4q24

OMIM:

 

617223

Gene summaries Genetic tests Medical literature

Select item 6172229.

#617222 - SUDDEN CARDIAC FAILURE, INFANTILE; SCFI

Cytogenetic locations: 4q24

OMIM:

 

617222

Gene summaries Genetic tests Medical literature

Select item 60024410.

*600244 - PROGRAMMED CELL DEATH 1; PDCD1

Cytogenetic locations: 2q37.3

OMIM:

 

600244

Gene summaries Genetic tests Medical literature

Select item 11500011.

115000 - CARDIAC ARRHYTHMIA

OMIM:

 

115000

Gene summaries Genetic tests Medical literature

Select item 10764012.

107640 - APNEA, CENTRAL SLEEP

OMIM:

 

107640

Gene summaries Genetic tests Medical literature

Select item 60471413.

*604714 - TSPY-LIKE 1; TSPYL1

Cytogenetic locations: 6q22.1

OMIM:

 

604714

Gene summaries Genetic tests Medical literature

Select item 60208714.

%602087 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4

Cytogenetic locations: 2q32.1-q32.3

OMIM:

 

602087

Gene summaries Genetic tests Medical literature

Select item 60016315.

*600163 - SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA SUBUNIT; SCN5A

Cytogenetic locations: 3p22.2

OMIM:

 

600163

Gene summaries Genetic tests Medical literature

Select item 61639916.

#616399 - BRUGADA SYNDROME 9; BRGDA9

Cytogenetic locations: 1p13.2

OMIM:

 

616399

Gene summaries Genetic tests Medical literature

Select item 61181817.

#611818 - LONG QT SYNDROME 9; LQT9

Cytogenetic locations: 3p25.3

OMIM:

 

611818

Gene summaries Genetic tests Medical literature

Select item 61014018.

#610140 - HEART-HAND SYNDROME, SLOVENIAN TYPE

OMIM:

 

610140

Gene summaries Genetic tests Medical literature

Select item 21250019.

#212500 - CATARACT 46, JUVENILE-ONSET; CTRCT46

Cytogenetic locations: 6p21.31

OMIM:

 

212500

Gene summaries Genetic tests Medical literature

Select item 23153020.

#231530 - 3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY

Cytogenetic locations: 4q25

OMIM:

 

231530

Gene summaries Genetic tests Medical literature