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Title : Warfarin - OMIM - NCBI
link : Warfarin - OMIM - NCBI

Warfarin - OMIM - NCBI

Warfarin - 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 "Warfarin" 

#122700 - COUMARIN RESISTANCE

COUMARIN SENSITIVITY, INCLUDED

Cytogenetic locations: 1pter-p36.13, 19q13.2, 1pter-p36.13, 16p11.2

OMIM:

 

122700

Gene summaries Genetic tests Medical literature

Select item 1186502.

118650 - CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT

CHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED

OMIM:

 

118650

Gene summaries Genetic tests Medical literature

Select item 6085473.

*608547 - VITAMIN K EPOXIDE REDUCTASE COMPLEX, SUBUNIT 1; VKORC1

Cytogenetic locations: 16p11.2

OMIM:

 

608547

Gene summaries Genetic tests Medical literature

Select item 6011304.

*601130 - CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9

Cytogenetic locations: 10q23.33

OMIM:

 

601130

Gene summaries Genetic tests Medical literature

Select item 1768605.

#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 3007466.

*300746 - COAGULATION FACTOR IX; F9

Cytogenetic locations: Xq27.1

OMIM:

 

300746

Gene summaries Genetic tests Medical literature

Select item 6123367.

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

Cytogenetic locations: 3q11.1

OMIM:

 

612336

Gene summaries Genetic tests Medical literature

Select item 6123098.

*612309 - COAGULATION FACTOR V; F5

FACTOR V LEIDEN, INCLUDED

Cytogenetic locations: 1q24.2

OMIM:

 

612309

Gene summaries Genetic tests Medical literature

Select item 6088389.

*608838 - VITAMIN K EPOXIDE REDUCTASE COMPLEX, SUBUNIT 1-LIKE 1; VKORC1L1

Cytogenetic locations: 7q11.21

OMIM:

 

608838

Gene summaries Genetic tests Medical literature

Select item 27745010.

#277450 - VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1

Cytogenetic locations: 2p11.2

OMIM:

 

277450

Gene summaries Genetic tests Medical literature

Select item 30000311.

*300003 - ARYLSULFATASE F; ARSF

Cytogenetic locations: Xp22.33

OMIM:

 

300003

Gene summaries Genetic tests Medical literature

Select item 60442612.

*604426 - CYTOCHROME P450, FAMILY 4, SUBFAMILY F, POLYPEPTIDE 2; CYP4F2

Cytogenetic locations: 19p13.12

OMIM:

 

604426

Gene summaries Genetic tests Medical literature

Select item 60747313.

#607473 - VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2

Cytogenetic locations: 16p11.2

OMIM:

 

607473

Gene summaries Genetic tests Medical literature

Select item 30018014.

*300180 - ARYLSULFATASE E; ARSE

Cytogenetic locations: Xp22.33

OMIM:

 

300180

Gene summaries Genetic tests Medical literature

Select item 61230415.

#612304 - THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4

Cytogenetic locations: 2q14.3

OMIM:

 

612304

Gene summaries Genetic tests Medical literature

Select item 30295016.

#302950 - CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE; CDPX1

Cytogenetic locations: Xp22.33

OMIM:

 

302950

Gene summaries Genetic tests Medical literature

Select item 15505017.

%155050 - MAXILLONASAL DYSPLASIA, BINDER TYPE

OMIM:

 

155050

Gene summaries Genetic tests Medical literature

Select item 24515018.

#245150 - KEUTEL SYNDROME; KTLS

Cytogenetic locations: 12p12.3

OMIM:

 

245150

Gene summaries Genetic tests Medical literature

Select item 60034119.

*600341 - TYRO3 PROTEIN TYROSINE KINASE; TYRO3

Cytogenetic locations: 15q15.1

OMIM:

 

600341

Gene summaries Genetic tests Medical literature

Select item 10913520.

*109135 - AXL RECEPTOR TYROSINE KINASE; AXL

Cytogenetic locations: 19q13.2

OMIM:

 

109135

Gene summaries Genetic tests Medical literature

Thus Article Warfarin - OMIM - NCBI

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