Related Entries for OMIM (Select 233700) - OMIM

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Links from OMIM

Items: 19

Select item 2337001.

#233700 - GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 1; CGD1

Cytogenetic locations: 12848318

OMIM:: 233700

Gene summaries Genetic tests Medical literature

Select item 6140792.

#614079 - ASPERGILLOSIS, SUSCEPTIBILITY TO

Cytogenetic locations: 1p36, 1p36

OMIM:: 614079

Gene summaries Genetic tests Medical literature

Select item 6085153.

*608515 - NEUTROPHIL CYTOSOLIC FACTOR 2; NCF2

Cytogenetic locations: 17803798

OMIM:: 608515

Gene summaries Genetic tests Medical literature

Select item 6085124.

*608512 - NEUTROPHIL CYTOSOLIC FACTOR 1; NCF1

Cytogenetic locations: 19916719

OMIM:: 608512

Gene summaries Genetic tests Medical literature

Select item 6085085.

*608508 - CYTOCHROME b(-245), ALPHA SUBUNIT; CYBA

Cytogenetic locations: Cholestasis

OMIM:: 608508

Gene summaries Genetic tests Medical literature

Select item 6031496.

*603149 - INTERLEUKIN 17A; IL17A

Cytogenetic locations: 22466287

OMIM:: 603149

Gene summaries Genetic tests Medical literature

Select item 3064007.

#306400 - GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CGDX

CYTOCHROME b-POSITIVE GRANULOMATOUS DISEASE, CHRONIC, X-LINKED, INCLUDED

Cytogenetic locations: 603107

OMIM:: 306400

Gene summaries Genetic tests Medical literature

Select item 3009088.

#300908 - ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 1; CNSHA1

Cytogenetic locations: CT47A9

OMIM:: 300908

Gene summaries Genetic tests Medical literature

Select item 3004819.

*300481 - CYTOCHROME b(-245), BETA SUBUNIT; CYBB

Cytogenetic locations: 603107

OMIM:: 300481

Gene summaries Genetic tests Medical literature

Select item 30029210.

*300292 - FORKHEAD BOX P3; FOXP3

Cytogenetic locations: Immunodeficiency

OMIM:: 300292

Gene summaries Genetic tests Medical literature

Select item 23590011.

%235900 - HISTIOCYTOSIS, FAMILIAL LIPOCHROME

OMIM:: 235900

Gene summaries Genetic tests Medical literature

Select item 23080012.

#230800 - GAUCHER DISEASE, TYPE I; GD1

Cytogenetic locations: 607377

OMIM:: 230800

Gene summaries Genetic tests Medical literature

Select item 20191013.

#201910 - ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

HYPERANDROGENISM, NONCLASSIC TYPE, DUE TO 21-HYDROXYLASE DEFICIENCY, INCLUDED

Cytogenetic locations: 17517053

OMIM:: 201910

Gene summaries Genetic tests Medical literature

Select item 19340014.

#193400 - VON WILLEBRAND DISEASE, TYPE 1; VWD1

Cytogenetic locations: 13100416

OMIM:: 193400

Gene summaries Genetic tests Medical literature

Select item 19116015.

*191160 - TUMOR NECROSIS FACTOR; TNF

Cytogenetic locations: 19920095

OMIM:: 191160

Gene summaries Genetic tests Medical literature

Select item 16156116.

*161561 - INTERLEUKIN 12B; IL12B

Cytogenetic locations: 17187052

OMIM:: 161561

Gene summaries Genetic tests Medical literature

Select item 15573017.

*155730 - CHEMOKINE, CXC MOTIF, LIGAND 1; CXCL1

Cytogenetic locations: 10714678

OMIM:: 155730

Gene summaries Genetic tests Medical literature

Select item 14757018.

*147570 - INTERFERON, GAMMA; IFNG

Cytogenetic locations: Hnrnpa1

OMIM:: 147570

Gene summaries Genetic tests Medical literature

Select item 14743519.

*147435 - INDOLEAMINE 2,3-DIOXYGENASE; IDO1

Cytogenetic locations: 20190767

OMIM:: 147435

Gene summaries Genetic tests Medical literature

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Related Entries for OMIM (Select 233700) (19)
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