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Title : Heart disease - OMIM - NCBI
link : Heart disease - OMIM - NCBI

Heart disease - OMIM - NCBI

Heart disease - 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 "Heart disease" 

218450 - CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS

OMIM:

 

218450

Gene summaries Genetic tests Medical literature

Select item 6029152.

*602915 - TRYPTOPHAN-RICH BASIC PROTEIN; WRB

Cytogenetic locations: 21q22.2

OMIM:

 

602915

Gene summaries Genetic tests Medical literature

Select item 2357503.

235750 - HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT

OMIM:

 

235750

Gene summaries Genetic tests Medical literature

Select item 6013554.

601355 - MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS, AND HYPOSEGMENTED LUNGS

OMIM:

 

601355

Gene summaries Genetic tests Medical literature

Select item 6082275.

608227 - CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRAL NEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION

OMIM:

 

608227

Gene summaries Genetic tests Medical literature

Select item 6120306.

%612030 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 9; CHDS9

Cytogenetic locations: 8p22

OMIM:

 

612030

Gene summaries Genetic tests Medical literature

Select item 3004647.

%300464 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 3

Cytogenetic locations: Xq23-q26

OMIM:

 

300464

Gene summaries Genetic tests Medical literature

Select item 6083188.

%608318 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 4

Cytogenetic locations: 14q32

OMIM:

 

608318

Gene summaries Genetic tests Medical literature

Select item 6042119.

604211 - HIRSCHSPRUNG DISEASE WITH HEART DEFECTS, LARYNGEAL ANOMALIES, AND PREAXIAL POLYDACTYLY

OMIM:

 

604211

Gene summaries Genetic tests Medical literature

Select item 60116510.

601165 - CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE

OMIM:

 

601165

Gene summaries Genetic tests Medical literature

Select item 26174011.

#261740 - GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL

Cytogenetic locations: 7q36.1

OMIM:

 

261740

Gene summaries Genetic tests Medical literature

Select item 60890112.

#608901 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5

Cytogenetic locations: 3q21.1-q21.2

OMIM:

 

608901

Gene summaries Genetic tests Medical literature

Select item 61093813.

#610938 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7; CHDS7

Cytogenetic locations: 7q21.11

OMIM:

 

610938

Gene summaries Genetic tests Medical literature

Select item 60831614.

%608316 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 2

Cytogenetic locations: 2q21.1-q22

OMIM:

 

608316

Gene summaries Genetic tests Medical literature

Select item 60733915.

%607339 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1

Cytogenetic locations: 1pter-p36.13, 16pter-p13

OMIM:

 

607339

Gene summaries Genetic tests Medical literature

Select item 11390016.

#113900 - PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A

HEART BLOCK, NONPROGRESSIVE, INCLUDED

Cytogenetic locations: 3p22.2

OMIM:

 

113900

Gene summaries Genetic tests Medical literature

Select item 61554217.

#615542 - TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD

Cytogenetic locations: 8p23.1

OMIM:

 

615542

Gene summaries Genetic tests Medical literature

Select item 24962018.

%249620 - OHDO SYNDROME

OMIM:

 

249620

Gene summaries Genetic tests Medical literature

Select item 60253119.

#602531 - GRANGE SYNDROME; GRNG

Cytogenetic locations: 1q22

OMIM:

 

602531

Gene summaries Genetic tests Medical literature

Select item 61446620.

#614466 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 6; CHDS6

Cytogenetic locations: 11q22.2

OMIM:

 

614466

Gene summaries Genetic tests Medical literature

Thus Article Heart disease - OMIM - NCBI

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