Depression - OMIM - NCBI

Depression - 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 "Depression" 

%608691 - MAJOR DEPRESSIVE DISORDER 2

Cytogenetic locations: 15q25.3-q26.2

OMIM:

 

608691

Gene summaries Genetic tests Medical literature

Select item 1686052.

#168605 - PERRY SYNDROME

Cytogenetic locations: 2p13.1

OMIM:

 

168605

Gene summaries Genetic tests Medical literature

Select item 6085203.

%608520 - MAJOR DEPRESSIVE DISORDER 1

Cytogenetic locations: 12q22-q23.2

OMIM:

 

608520

Gene summaries Genetic tests Medical literature

Select item 2698804.

#269880 - SHORT SYNDROME

Cytogenetic locations: 5q13.1

OMIM:

 

269880

Gene summaries Genetic tests Medical literature

Select item 6085165.

#608516 - MAJOR DEPRESSIVE DISORDER; MDD

SEASONAL AFFECTIVE DISORDER, INCLUDED; SAD, INCLUDED

Cytogenetic locations: 13q14.2, 1pter-p36.13, 12q22-q23.2, 1pter-p36.13, 12q21.1

OMIM:

 

608516

Gene summaries Genetic tests Medical literature

Select item 2155506.

215550 - CIRCUMVALLATE PLACENTA SYNDROME

OMIM:

 

215550

Gene summaries Genetic tests Medical literature

Select item 6074787.

*607478 - TRYPTOPHAN HYDROXYLASE 2; TPH2

Cytogenetic locations: 12q21.1

OMIM:

 

607478

Gene summaries Genetic tests Medical literature

Select item 1210708.

121070 - ARTHROGRYPOSIS, DISTAL, TYPE 2E

OMIM:

 

121070

Gene summaries Genetic tests Medical literature

Select item 2446009.

244600 - KERATOCONUS POSTICUS CIRCUMSCRIPTUS; KPC

KPC WITH ASSOCIATED MALFORMATIONS, INCLUDED

OMIM:

 

244600

Gene summaries Genetic tests Medical literature

Select item 17250010.

172500 - PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION

OMIM:

 

172500

Gene summaries Genetic tests Medical literature

Select item 61688211.

#616882 - ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3; FASPS3

Cytogenetic locations: 1p36.23

OMIM:

 

616882

Gene summaries Genetic tests Medical literature

Select item 61641312.

#616413 - BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6

Cytogenetic locations: 1q25.3

OMIM:

 

616413

Gene summaries Genetic tests Medical literature

Select item 60320413.

%603204 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2

Cytogenetic locations: 15q24

OMIM:

 

603204

Gene summaries Genetic tests Medical literature

Select item 60928614.

#609286 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3

Cytogenetic locations: 10q24.31

OMIM:

 

609286

Gene summaries Genetic tests Medical literature

Select item 60412115.

#604121 - CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN

Cytogenetic locations: 19p13.2

OMIM:

 

604121

Gene summaries Genetic tests Medical literature

Select item 61548316.

#615483 - BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5

Cytogenetic locations: 22q13.1

OMIM:

 

615483

Gene summaries Genetic tests Medical literature

Select item 61545817.

#615458 - MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT

Cytogenetic locations: 16q23.1

OMIM:

 

615458

Gene summaries Genetic tests Medical literature

Select item 26505018.

#265050 - 3MC SYNDROME 2; 3MC2

Cytogenetic locations: 2p25.3

OMIM:

 

265050

Gene summaries Genetic tests Medical literature

Select item 61639819.

#616398 - DYSTONIA 26, MYOCLONIC; DYT26

Cytogenetic locations: 22q12.3

OMIM:

 

616398

Gene summaries Genetic tests Medical literature

Select item 61500520.

#615005 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5

Cytogenetic locations: 9q34.3

OMIM:

 

615005

Gene summaries Genetic tests Medical literature