Hemophilia - OMIM - NCBI

Hemophilia - 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 "Hemophilia" 

306800 - HEMOPHILIA A WITH VASCULAR ABNORMALITY

OMIM:

 

306800

Gene summaries Genetic tests Medical literature

Select item 1345002.

134500 - FACTOR VIII DEFICIENCY

OMIM:

 

134500

Gene summaries Genetic tests Medical literature

Select item 3069003.

#306900 - HEMOPHILIA B; HEMB

HEMOPHILIA B(M), INCLUDED

Cytogenetic locations: Xq27.1

OMIM:

 

306900

Gene summaries Genetic tests Medical literature

Select item 3067004.

#306700 - HEMOPHILIA A; HEMA

Cytogenetic locations: Xq28

OMIM:

 

306700

Gene summaries Genetic tests Medical literature

Select item 3008415.

*300841 - COAGULATION FACTOR VIII; F8

Cytogenetic locations: Xq28

OMIM:

 

300841

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 3145607.

314560 - VON WILLEBRAND DISEASE, X-LINKED FORM

OMIM:

 

314560

Gene summaries Genetic tests Medical literature

Select item 1345408.

134540 - FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF

OMIM:

 

134540

Gene summaries Genetic tests Medical literature

Select item 1428309.

+142830 - MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, B; HLA-B

ABACAVIR HYPERSENSITIVITY, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 6p21.33

OMIM:

 

142830

Gene summaries Genetic tests Medical literature

Select item 14778110.

*147781 - INTERLEUKIN 4 RECEPTOR; IL4R

Cytogenetic locations: 16p12.1

OMIM:

 

147781

Gene summaries Genetic tests Medical literature

Select item 27748011.

#277480 - VON WILLEBRAND DISEASE, TYPE 3; VWD3

Cytogenetic locations: 12p13.31

OMIM:

 

277480

Gene summaries Genetic tests Medical literature

Select item 19340012.

#193400 - VON WILLEBRAND DISEASE, TYPE 1; VWD1

Cytogenetic locations: 12p13.31

OMIM:

 

193400

Gene summaries Genetic tests Medical literature

Select item 23400013.

#234000 - FACTOR XII DEFICIENCY

Cytogenetic locations: 5q35.3

OMIM:

 

234000

Gene summaries Genetic tests Medical literature

Select item 22730014.

#227300 - FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1; F5F8D1

Cytogenetic locations: 18q21.32

OMIM:

 

227300

Gene summaries Genetic tests Medical literature

Select item 17361015.

*173610 - SELECTIN P; SELP

Cytogenetic locations: 1q24.2

OMIM:

 

173610

Gene summaries Genetic tests Medical literature

Select item 61355416.

#613554 - VON WILLEBRAND DISEASE, TYPE 2; VWD2

VON WILLEBRAND DISEASE, TYPE 2A, INCLUDED; VWD2A, INCLUDED

Cytogenetic locations: 12p13.31

OMIM:

 

613554

Gene summaries Genetic tests Medical literature

Select item 60942317.

#609423 - HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RESISTANCE TO, INCLUDED

Cytogenetic locations: 1pter-p36.13, 1q32.1, 1pter-p36.13, 17q12, 1pter-p36.13, 17q12, 1pter-p36.13, 17q12, 1pter-p36.13, 17q11.2, 1pter-p36.13, 16p12.1, 1pter-p36.13, 12q15

OMIM:

 

609423

Gene summaries Genetic tests Medical literature

Select item 61316018.

*613160 - VON WILLEBRAND FACTOR; VWF

Cytogenetic locations: 12p13.31

OMIM:

 

613160

Gene summaries Genetic tests Medical literature

Select item 30062419.

#300624 - FRAGILE X SYNDROME; FXS

Cytogenetic locations: Xq27.3

OMIM:

 

300624

Gene summaries Genetic tests Medical literature

Select item 30590020.

*305900 - GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD

Cytogenetic locations: Xq28

OMIM:

 

305900

Gene summaries Genetic tests Medical literature