Behavior - OMIM - NCBI

Behavior - 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 "Behavior" 

240000 - HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE

OMIM:

 

240000

Gene summaries Genetic tests Medical literature

Select item 3004912.

#300491 - EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR DISORDERS

Cytogenetic locations: Xp11.3-p11.2

OMIM:

 

300491

Gene summaries Genetic tests Medical literature

Select item 3006153.

#300615 - BRUNNER SYNDROME; BRNRS

ANTISOCIAL BEHAVIOR, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: Xp11.3

OMIM:

 

300615

Gene summaries Genetic tests Medical literature

Select item 3004384.

#300438 - HSD10 MITOCHONDRIAL DISEASE; HSD10MD

Cytogenetic locations: Xp11.22

OMIM:

 

300438

Gene summaries Genetic tests Medical literature

Select item 6016965.

601696 - NOVELTY SEEKING PERSONALITY TRAIT

RISK-TAKING BEHAVIOR, INCLUDED

Cytogenetic locations: 11p15.5

OMIM:

 

601696

Gene summaries Genetic tests Medical literature

Select item 3098506.

*309850 - MONOAMINE OXIDASE A; MAOA

Cytogenetic locations: Xp11.3

OMIM:

 

309850

Gene summaries Genetic tests Medical literature

Select item 3004947.

#300494 - ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1

Cytogenetic locations: Xq13.1

OMIM:

 

300494

Gene summaries Genetic tests Medical literature

Select item 3004978.

#300497 - ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2

Cytogenetic locations: Xp22.32-p22.31

OMIM:

 

300497

Gene summaries Genetic tests Medical literature

Select item 3004549.

%300454 - MENTAL RETARDATION, X-LINKED 77; MRX77

Cytogenetic locations: Xq12-q21.3

OMIM:

 

300454

Gene summaries Genetic tests Medical literature

Select item 30984010.

309840 - MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS

OMIM:

 

309840

Gene summaries Genetic tests Medical literature

Select item 31344011.

*313440 - SYNAPSIN I; SYN1

Cytogenetic locations: Xp11.3-p11.2

OMIM:

 

313440

Gene summaries Genetic tests Medical literature

Select item 61322912.

#613229 - TRICHOTILLOMANIA; TTM

Cytogenetic locations: 13q31.1

OMIM:

 

613229

Gene summaries Genetic tests Medical literature

Select item 60737313.

%607373 - AUTISM, SUSCEPTIBILITY TO, 8; AUTS8

Cytogenetic locations: 3q25-q27

OMIM:

 

607373

Gene summaries Genetic tests Medical literature

Select item 30049614.

#300496 - AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3

Cytogenetic locations: Xq28

OMIM:

 

300496

Gene summaries Genetic tests Medical literature

Select item 30042515.

#300425 - AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1

Cytogenetic locations: Xq13.1

OMIM:

 

300425

Gene summaries Genetic tests Medical literature

Select item 22912016.

%229120 - FOUNTAIN SYNDROME

OMIM:

 

229120

Gene summaries Genetic tests Medical literature

Select item 60804917.

%608049 - AUTISM, SUSCEPTIBILITY TO, 3; AUTS3

Cytogenetic locations: 13q14.2-q14.1

OMIM:

 

608049

Gene summaries Genetic tests Medical literature

Select item 61582818.

#615828 - MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24

Cytogenetic locations: 11p15.5

OMIM:

 

615828

Gene summaries Genetic tests Medical literature

Select item 60863119.

%608631 - ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2

Cytogenetic locations: 17p13

OMIM:

 

608631

Gene summaries Genetic tests Medical literature

Select item 60863820.

%608638 - ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1

Cytogenetic locations: 3q25-q27

OMIM:

 

608638

Gene summaries Genetic tests Medical literature