Sepsis - OMIM - NCBI

Sepsis - 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 "Sepsis" 

*608633 - CASPASE 12, APOPTOSIS-RELATED CYSTEINE PROTEASE; CASP12

Cytogenetic locations: 11q22.3

OMIM:

 

608633

Gene summaries Genetic tests Medical literature

Select item 6106802.

610680 - HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS

OMIM:

 

610680

Gene summaries Genetic tests Medical literature

Select item 2714003.

#271400 - ASPLENIA, ISOLATED CONGENITAL; ICAS

Cytogenetic locations: 3p22.1

OMIM:

 

271400

Gene summaries Genetic tests Medical literature

Select item 2304004.

#230400 - GALACTOSEMIA

GALACTOSEMIA, DUARTE VARIANT, INCLUDED

Cytogenetic locations: 9p13.3

OMIM:

 

230400

Gene summaries Genetic tests Medical literature

Select item 6148865.

#614886 - PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER); PBD12A

PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 14, INCLUDED

Cytogenetic locations: 1q23.2

OMIM:

 

614886

Gene summaries Genetic tests Medical literature

Select item 6125416.

#612541 - NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4

DURSUN SYNDROME, INCLUDED

Cytogenetic locations: 17q21.31

OMIM:

 

612541

Gene summaries Genetic tests Medical literature

Select item 6047777.

#604777 - ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5

Cytogenetic locations: 19p13.12

OMIM:

 

604777

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 1764509.

#176450 - CURRARINO SYNDROME

SACRAL AGENESIS SYNDROME, INCLUDED

Cytogenetic locations: 7q36.3

OMIM:

 

176450

Gene summaries Genetic tests Medical literature

Select item 13176010.

#131760 - EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE; EBSDM

Cytogenetic locations: 1pter-p36.13, 17q21.2

OMIM:

 

131760

Gene summaries Genetic tests Medical literature

Select item 61473911.

#614739 - 3-@METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL

Cytogenetic locations: 6q25.3

OMIM:

 

614739

Gene summaries Genetic tests Medical literature

Select item 24250012.

#242500 - ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B

Cytogenetic locations: 2q35

OMIM:

 

242500

Gene summaries Genetic tests Medical literature

Select item 61340413.

#613404 - ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2; ARCS2

Cytogenetic locations: 14q24.3

OMIM:

 

613404

Gene summaries Genetic tests Medical literature

Select item 20808514.

#208085 - ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1; ARCS1

Cytogenetic locations: 15q26.1

OMIM:

 

208085

Gene summaries Genetic tests Medical literature

Select item 60994915.

*609949 - COMPLEMENT COMPONENT 5a RECEPTOR 2; C5AR2

Cytogenetic locations: 19q13.32

OMIM:

 

609949

Gene summaries Genetic tests Medical literature

Select item 15199016.

*151990 - LIPOPOLYSACCHARIDE-BINDING PROTEIN; LBP

Cytogenetic locations: 20q11.23

OMIM:

 

151990

Gene summaries Genetic tests Medical literature

Select item 21703017.

*217030 - COMPLEMENT FACTOR I; CFI

Cytogenetic locations: 4q25

OMIM:

 

217030

Gene summaries Genetic tests Medical literature

Select item 17332518.

*173325 - JUNCTION PLAKOGLOBIN; JUP

Cytogenetic locations: 17q21.2

OMIM:

 

173325

Gene summaries Genetic tests Medical literature

Select item 13463719.

*134637 - FAS CELL SURFACE DEATH RECEPTOR; FAS

Cytogenetic locations: 10q23.31

OMIM:

 

134637

Gene summaries Genetic tests Medical literature

Select item 61546920.

*615469 - MICRO RNA 574; MIR574

MICRO RNA 574-3p, INCLUDED; MIR574-3p, INCLUDED

Cytogenetic locations: 4p14

OMIM:

 

615469

Gene summaries Genetic tests Medical literature