Chronic fatigue syndrome - OMIM - NCBI

Chronic fatigue syndrome - 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 "Chronic fatigue syndrome" 

#604715 - ORTHOSTATIC INTOLERANCE

Cytogenetic locations: 16q12.2

OMIM:

 

604715

Gene summaries Genetic tests Medical literature

Select item 1441202.

144120 - HYPERIMMUNOGLOBULIN G1(A1) SYNDROME

Cytogenetic locations: 14q32.33

OMIM:

 

144120

Gene summaries Genetic tests Medical literature

Select item 1919003.

#191900 - MUCKLE-WELLS SYNDROME; MWS

Cytogenetic locations: 1q44

OMIM:

 

191900

Gene summaries Genetic tests Medical literature

Select item 6025224.

#602522 - BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A

SENSORINEURAL DEAFNESS WITH MILD RENAL DYSFUNCTION, INCLUDED

Cytogenetic locations: 1p32.3

OMIM:

 

602522

Gene summaries Genetic tests Medical literature

Select item 3020605.

#302060 - BARTH SYNDROME; BTHS

Cytogenetic locations: Xq28

OMIM:

 

302060

Gene summaries Genetic tests Medical literature

Select item 6067776.

#606777 - GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1

GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED

Cytogenetic locations: 1p34.2

OMIM:

 

606777

Gene summaries Genetic tests Medical literature

Select item 1638007.

#163800 - SICK SINUS SYNDROME 2; SSS2

Cytogenetic locations: 15q24.1

OMIM:

 

163800

Gene summaries Genetic tests Medical literature

Select item 2375008.

#237500 - DUBIN-JOHNSON SYNDROME; DJS

Cytogenetic locations: 10q24.2

OMIM:

 

237500

Gene summaries Genetic tests Medical literature

Select item 2115309.

#211530 - BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1

Cytogenetic locations: 20p13

OMIM:

 

211530

Gene summaries Genetic tests Medical literature

Select item 15560010.

%155600 - MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1; CMM1

Cytogenetic locations: 1p36

OMIM:

 

155600

Gene summaries Genetic tests Medical literature

Select item 19438011.

#194380 - DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1

Cytogenetic locations: 16q24.3

OMIM:

 

194380

Gene summaries Genetic tests Medical literature

Select item 61148912.

#611489 - CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY

CORTICOSTEROID-BINDING GLOBULIN, ELEVATED, INCLUDED

Cytogenetic locations: 14q32.13

OMIM:

 

611489

Gene summaries Genetic tests Medical literature

Select item 61596213.

#615962 - GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR

Cytogenetic locations: 5q31.3

OMIM:

 

615962

Gene summaries Genetic tests Medical literature

Select item 26048014.

260480 - PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX

OMIM:

 

260480

Gene summaries Genetic tests Medical literature

Select item 30150015.

#301500 - FABRY DISEASE

FABRY DISEASE, CARDIAC VARIANT, INCLUDED

Cytogenetic locations: Xq22.1

OMIM:

 

301500

Gene summaries Genetic tests Medical literature

Select item 60390316.

#603903 - SICKLE CELL ANEMIA

Cytogenetic locations: 11p15.4

OMIM:

 

603903

Gene summaries Genetic tests Medical literature

Select item 17040017.

#170400 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1

Cytogenetic locations: 1q32.1

OMIM:

 

170400

Gene summaries Genetic tests Medical literature

Select item 12250018.

*122500 - SERPIN PEPTIDASE INHIBITOR, CLADE A, MEMBER 6; SERPINA6

Cytogenetic locations: 14q32.13

OMIM:

 

122500

Gene summaries Genetic tests Medical literature

Select item 18825019.

*188250 - THYMIDINE KINASE, MITOCHONDRIAL; TK2

Cytogenetic locations: 16q21

OMIM:

 

188250

Gene summaries Genetic tests Medical literature

Select item 60592120.

*605921 - STROMAL INTERACTION MOLECULE 1; STIM1

Cytogenetic locations: 11p15.4

OMIM:

 

605921

Gene summaries Genetic tests Medical literature