Meningitis - OMIM - NCBI

Meningitis - 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 "Meningitis" 

1.

%308250 - IMMUNOGLOBULIN M, LEVEL OF

OMIM:

 

308250

Gene summaries Genetic tests Medical literature

Select item 6071152.

#607115 - CINCA SYNDROME; CINCA

Cytogenetic locations: 1q44

OMIM:

 

607115

Gene summaries Genetic tests Medical literature

Select item 6135003.

#613500 - AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2

Cytogenetic locations: 22q11.23

OMIM:

 

613500

Gene summaries Genetic tests Medical literature

Select item 6137904.

#613790 - COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I; C8D1

Cytogenetic locations: 1p32.2

OMIM:

 

613790

Gene summaries Genetic tests Medical literature

Select item 6109845.

#610984 - COMPLEMENT FACTOR I DEFICIENCY; CFID

Cytogenetic locations: 4q25

OMIM:

 

610984

Gene summaries Genetic tests Medical literature

Select item 2491006.

#249100 - FAMILIAL MEDITERRANEAN FEVER; FMF

Cytogenetic locations: 16p13.3

OMIM:

 

249100

Gene summaries Genetic tests Medical literature

Select item 6137897.

#613789 - COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2

Cytogenetic locations: 1p32.2

OMIM:

 

613789

Gene summaries Genetic tests Medical literature

Select item 6170538.

#617053 - MIRAGE SYNDROME; MIRAGE

Cytogenetic locations: 7q21.2

OMIM:

 

617053

Gene summaries Genetic tests Medical literature

Select item 2120509.

#212050 - CANDIDIASIS, FAMILIAL, 2; CANDF2

Cytogenetic locations: 9q34.3

OMIM:

 

212050

Gene summaries Genetic tests Medical literature

Select item 60014510.

#600145 - SACRAL DEFECT WITH ANTERIOR MENINGOCELE

CAUDAL DYSGENESIS SYNDROME, INCLUDED

Cytogenetic locations: 1p13.1

OMIM:

 

600145

Gene summaries Genetic tests Medical literature

Select item 61300211.

#613002 - ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2

Cytogenetic locations: 4q35.1

OMIM:

 

613002

Gene summaries Genetic tests Medical literature

Select item 60090312.

600903 - WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM

OMIM:

 

600903

Gene summaries Genetic tests Medical literature

Select item 60080213.

#600802 - SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE

Cytogenetic locations: 19p13.11

OMIM:

 

600802

Gene summaries Genetic tests Medical literature

Select item 61790014.

#617900 - ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8

Cytogenetic locations: 12q14.2

OMIM:

 

617900

Gene summaries Genetic tests Medical literature

Select item 24050015.

#240500 - IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2

Cytogenetic locations: 17p11.2

OMIM:

 

240500

Gene summaries Genetic tests Medical literature

Select item 30720016.

#307200 - ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3

Cytogenetic locations: Xq22.1

OMIM:

 

307200

Gene summaries Genetic tests Medical literature

Select item 60355317.

#603553 - HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2; FHL2

Cytogenetic locations: 10q22.1

OMIM:

 

603553

Gene summaries Genetic tests Medical literature

Select item 60145718.

#601457 - SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE

Cytogenetic locations: 1pter-p36.13, 11p12

OMIM:

 

601457

Gene summaries Genetic tests Medical literature

Select item 20992019.

#209920 - BARE LYMPHOCYTE SYNDROME, TYPE II

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A, INCLUDED

Cytogenetic locations: 1pter-p36.13, 13q13.3, 1pter-p36.13, 1q21.3

OMIM:

 

209920

Gene summaries Genetic tests Medical literature

Select item 26770020.

%267700 - HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1; FHL1

Cytogenetic locations: 9q21.3-q22

OMIM:

 

267700

Gene summaries Genetic tests Medical literature