Venous thromboembolism - OMIM - NCBI

Venous thromboembolism - 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 "Venous thromboembolism" 

#188050 - THROMBOPHILIA DUE TO THROMBIN DEFECT; THPH1

THROMBOSIS, PROTECTION AGAINST, INCLUDED

Cytogenetic locations: 1pter-p36.13, 1p36.22, 1pter-p36.13, 6p25.1

OMIM:

 

188050

Gene summaries Genetic tests Medical literature

Select item 1768602.

#176860 - THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT; THPH3

PROTEIN C DEFICIENCY, ACQUIRED, INCLUDED

Cytogenetic locations: 2q14.3

OMIM:

 

176860

Gene summaries Genetic tests Medical literature

Select item 6039243.

*603924 - HYALURONAN-BINDING PROTEIN 2; HABP2

Cytogenetic locations: 10q25.3

OMIM:

 

603924

Gene summaries Genetic tests Medical literature

Select item 6123364.

#612336 - THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT; THPH5

Cytogenetic locations: 3q11.1

OMIM:

 

612336

Gene summaries Genetic tests Medical literature

Select item 6070935.

*607093 - 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR

Cytogenetic locations: 1p36.22

OMIM:

 

607093

Gene summaries Genetic tests Medical literature

Select item 1880556.

#188055 - THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE; THPH2

THROMBOPHILIA DUE TO FACTOR V LEIDEN, INCLUDED

Cytogenetic locations: 1q24.2

OMIM:

 

188055

Gene summaries Genetic tests Medical literature

Select item 3007467.

*300746 - COAGULATION FACTOR IX; F9

Cytogenetic locations: Xq27.1

OMIM:

 

300746

Gene summaries Genetic tests Medical literature

Select item 1073208.

107320 - ANTIPHOSPHOLIPID SYNDROME, FAMILIAL

Cytogenetic locations: 6p21.3

OMIM:

 

107320

Gene summaries Genetic tests Medical literature

Select item 1769309.

*176930 - COAGULATION FACTOR II; F2

Cytogenetic locations: 11p11.2

OMIM:

 

176930

Gene summaries Genetic tests Medical literature

Select item 61230910.

*612309 - COAGULATION FACTOR V; F5

FACTOR V LEIDEN, INCLUDED

Cytogenetic locations: 1q24.2

OMIM:

 

612309

Gene summaries Genetic tests Medical literature

Select item 10730011.

*107300 - SERPIN PEPTIDASE INHIBITOR, CLADE C (ANTITHROMBIN), MEMBER 1; SERPINC1

Cytogenetic locations: 1q25.1

OMIM:

 

107300

Gene summaries Genetic tests Medical literature

Select item 23620012.

#236200 - HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY

HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED, INCLUDED

Cytogenetic locations: 21q22.3

OMIM:

 

236200

Gene summaries Genetic tests Medical literature

Select item 27740013.

#277400 - METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC, INCLUDED

Cytogenetic locations: 1pter-p36.13, 1p34.1

OMIM:

 

277400

Gene summaries Genetic tests Medical literature

Select item 17692014.

#176920 - PROTEUS SYNDROME

ELATTOPROTEUS SYNDROME, INCLUDED

Cytogenetic locations: 14q32.33

OMIM:

 

176920

Gene summaries Genetic tests Medical literature

Select item 61311615.

#613116 - THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY; THPH11

THROMBOPHILIA DUE TO ELEVATED HISTIDINE-RICH GLYCOPROTEIN, INCLUDED

Cytogenetic locations: 3q27.3

OMIM:

 

613116

Gene summaries Genetic tests Medical literature

Select item 61228316.

*612283 - PROTEIN C; PROC

Cytogenetic locations: 2q14.3

OMIM:

 

612283

Gene summaries Genetic tests Medical literature

Select item 13482017.

*134820 - FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA

Cytogenetic locations: 4q31.3

OMIM:

 

134820

Gene summaries Genetic tests Medical literature

Select item 17335018.

*173350 - PLASMINOGEN; PLG

ANGIOSTATIN, INCLUDED

Cytogenetic locations: 6q26

OMIM:

 

173350

Gene summaries Genetic tests Medical literature

Select item 61311819.

#613118 - ANTITHROMBIN III DEFICIENCY; AT3D

Cytogenetic locations: 1q25.1

OMIM:

 

613118

Gene summaries Genetic tests Medical literature

Select item 61424220.

*614242 - SOLUTE CARRIER FAMILY 16 (MONOCARBOXYLIC ACID TRANSPORTER), MEMBER 9; SLC16A9

Cytogenetic locations: 10q21.2

OMIM:

 

614242

Gene summaries Genetic tests Medical literature