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Title : Nutrition or nutrigenomics - OMIM - NCBI
link : Nutrition or nutrigenomics - OMIM - NCBI

Nutrition or nutrigenomics - OMIM - NCBI

Nutrition or nutrigenomics - 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 "Nutrition or nutrigenomics " 

#615237 - CONGENITAL SHORT BOWEL SYNDROME; CSBS

Cytogenetic locations: 11q24.1

OMIM:

 

615237

Gene summaries Genetic tests Medical literature

Select item 2224702.

#222470 - TRICHOHEPATOENTERIC SYNDROME 1; THES1

Cytogenetic locations: 5q15

OMIM:

 

222470

Gene summaries Genetic tests Medical literature

Select item 6146023.

#614602 - TRICHOHEPATOENTERIC SYNDROME 2; THES2

Cytogenetic locations: 6p21.33

OMIM:

 

614602

Gene summaries Genetic tests Medical literature

Select item 6162014.

#616201 - CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID

Cytogenetic locations: 3p24.3

OMIM:

 

616201

Gene summaries Genetic tests Medical literature

Select item 6132175.

#613217 - DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5

Cytogenetic locations: 2p21

OMIM:

 

613217

Gene summaries Genetic tests Medical literature

Select item 1553106.

#155310 - VISCERAL MYOPATHY; VSCM

Cytogenetic locations: 2p13.1

OMIM:

 

155310

Gene summaries Genetic tests Medical literature

Select item 2266007.

#226600 - EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB

EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATA VARIANT, INCLUDED

Cytogenetic locations: 1pter-p36.13, 3p21.31

OMIM:

 

226600

Gene summaries Genetic tests Medical literature

Select item 2464508.

#246450 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD

Cytogenetic locations: 1p36.11

OMIM:

 

246450

Gene summaries Genetic tests Medical literature

Select item 1747639.

*174763 - POLYMERASE, DNA, GAMMA; POLG

Cytogenetic locations: 15q26.1

OMIM:

 

174763

Gene summaries Genetic tests Medical literature

Select item 61416410.

%614164 - GLUTATHIONE PEROXIDASE DEFICIENCY; GPXD

Cytogenetic locations: 3p21.31

OMIM:

 

614164

Gene summaries Genetic tests Medical literature

Select item 22310011.

#223100 - LACTOSE INTOLERANCE, ADULT TYPE

LACTASE PERSISTENCE, INCLUDED

Cytogenetic locations: 2q21.3

OMIM:

 

223100

Gene summaries Genetic tests Medical literature

Select item 60352312.

603523 - CHYLOTHORAX, CONGENITAL

OMIM:

 

603523

Gene summaries Genetic tests Medical literature

Select item 61037013.

#610370 - DIARRHEA 4, MALABSORPTIVE, CONGENITAL; DIAR4

Cytogenetic locations: 10q22.1

OMIM:

 

610370

Gene summaries Genetic tests Medical literature

Select item 61383114.

*613831 - UBIQUITIN PROTEIN LIGASE E3 COMPONENT N-RECOGNIN 3; UBR3

Cytogenetic locations: 2q31.1

OMIM:

 

613831

Gene summaries Genetic tests Medical literature

Select item 60429115.

604291 - ASCARIS LUMBRICOIDES INFECTION, SUSCEPTIBILITY TO

OMIM:

 

604291

Gene summaries Genetic tests Medical literature

Select item 61366216.

#613662 - MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B

Cytogenetic locations: 15q26.1

OMIM:

 

613662

Gene summaries Genetic tests Medical literature

Select item 10780017.

107800 - ARCUS CORNEAE

OMIM:

 

107800

Gene summaries Genetic tests Medical literature

Select item 25185018.

#251850 - DIARRHEA 2, WITH MICROVILLUS ATROPHY; DIAR2

Cytogenetic locations: 18q21.1

OMIM:

 

251850

Gene summaries Genetic tests Medical literature

Select item 10254519.

*102545 - ACTIN, GAMMA-2, SMOOTH MUSCLE, ENTERIC; ACTG2

Cytogenetic locations: 2p13.1

OMIM:

 

102545

Gene summaries Genetic tests Medical literature

Select item 60654020.

*606540 - MYOSIN VB; MYO5B

Cytogenetic locations: 18q21.1

OMIM:

 

606540

Gene summaries Genetic tests Medical literature

Thus Article Nutrition or nutrigenomics - OMIM - NCBI

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