Heart failure - OMIM - NCBI

Heart failure - OMIM - NCBI



From NIH OMIM

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

---

• Search OMIM for "Heart failure" 

+104250 - ALPHA-2C-ADRENERGIC RECEPTOR; ADRA2C

CONGESTIVE HEART FAILURE AND BETA-BLOCKER RESPONSE, MODIFIER OF, INCLUDED

Cytogenetic locations: 4p16.3

OMIM:

 

104250

Gene summaries Genetic tests Medical literature

Select item 1096302.

+109630 - BETA-1-ADRENERGIC RECEPTOR; ADRB1

CONGESTIVE HEART FAILURE AND BETA-BLOCKER RESPONSE, MODIFIER OF, INCLUDED

Cytogenetic locations: 10q25.3

OMIM:

 

109630

Gene summaries Genetic tests Medical literature

Select item 6157033.

#615703 - MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF

Cytogenetic locations: 3q29

OMIM:

 

615703

Gene summaries Genetic tests Medical literature

Select item 6172234.

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

Cytogenetic locations: 4q24

OMIM:

 

617223

Gene summaries Genetic tests Medical literature

Select item 6172225.

#617222 - SUDDEN CARDIAC FAILURE, INFANTILE; SCFI

Cytogenetic locations: 4q24

OMIM:

 

617222

Gene summaries Genetic tests Medical literature

Select item 2121126.

#212112 - CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM

OMIM:

 

212112

Gene summaries Genetic tests Medical literature

Select item 6105057.

#610505 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3; COXPD3

Cytogenetic locations: 12q14.1

OMIM:

 

610505

Gene summaries Genetic tests Medical literature

Select item 2532508.

#253250 - MULIBREY NANISM

Cytogenetic locations: 17q22

OMIM:

 

253250

Gene summaries Genetic tests Medical literature

Select item 1061809.

+106180 - ANGIOTENSIN I-CONVERTING ENZYME; ACE

ANGIOTENSIN I-CONVERTING ENZYME, PLASMA LEVEL OF, INCLUDED

Cytogenetic locations: 17q23.3

OMIM:

 

106180

Gene summaries Genetic tests Medical literature

Select item 20988010.

#209880 - CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS

ONDINE-HIRSCHSPRUNG DISEASE, INCLUDED; OHD, INCLUDED

Cytogenetic locations: 1pter-p36.13, 4p13, 1pter-p36.13, 20q13.32, 1pter-p36.13, 12q23.2

OMIM:

 

209880

Gene summaries Genetic tests Medical literature

Select item 10615011.

+106150 - ANGIOTENSINOGEN; AGT

IgA NEPHROPATHY, PROGRESSION TO RENAL FAILURE IN, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 1q42.2

OMIM:

 

106150

Gene summaries Genetic tests Medical literature

Select item 26174012.

#261740 - GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL

Cytogenetic locations: 7q36.1

OMIM:

 

261740

Gene summaries Genetic tests Medical literature

Select item 61747813.

#617478 - STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA

Cytogenetic locations: 1pter-p36.13, 14q22.3

OMIM:

 

617478

Gene summaries Genetic tests Medical literature

Select item 61760214.

#617602 - CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM

Cytogenetic locations: 9q34.12

OMIM:

 

617602

Gene summaries Genetic tests Medical literature

Select item 60000115.

#600001 - HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA

Cytogenetic locations: 18q11.2

OMIM:

 

600001

Gene summaries Genetic tests Medical literature

Select item 31440016.

#314400 - CARDIAC VALVULAR DYSPLASIA, X-LINKED; CVD1

OMIM:

 

314400

Gene summaries Genetic tests Medical literature

Select item 31190017.

#311900 - TARP SYNDROME; TARPS

Cytogenetic locations: Xp11.3

OMIM:

 

311900

Gene summaries Genetic tests Medical literature

Select item 60416918.

#604169 - LEFT VENTRICULAR NONCOMPACTION 1; LVNC1

Cytogenetic locations: 18q12.1

OMIM:

 

604169

Gene summaries Genetic tests Medical literature

Select item 61498019.

#614980 - CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2

Cytogenetic locations: 6q25.1

OMIM:

 

614980

Gene summaries Genetic tests Medical literature

Select item 30695520.

#306955 - HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED, INCLUDED; CHTD1, INCLUDED

Cytogenetic locations: Xq26.3

OMIM:

 

306955

Gene summaries Genetic tests Medical literature