Attention deficit hyperactivity disorder - OMIM - NCBI

Attention deficit hyperactivity disorder - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

---

• Search OMIM for "Attention deficit hyperactivity disorder" 

%608906 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 4

Cytogenetic locations: 5p13

OMIM:

 

608906

Gene summaries Genetic tests Medical literature

Select item 6089052.

%608905 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 3

Cytogenetic locations: 6q12

OMIM:

 

608905

Gene summaries Genetic tests Medical literature

Select item 6089033.

%608903 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 1

Cytogenetic locations: 16p13

OMIM:

 

608903

Gene summaries Genetic tests Medical literature

Select item 6123114.

%612311 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 5

Cytogenetic locations: 2q21.1

OMIM:

 

612311

Gene summaries Genetic tests Medical literature

Select item 6123125.

%612312 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 6

Cytogenetic locations: 13q12.11

OMIM:

 

612312

Gene summaries Genetic tests Medical literature

Select item 6089046.

%608904 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 2

Cytogenetic locations: 17p11

OMIM:

 

608904

Gene summaries Genetic tests Medical literature

Select item 6130037.

#613003 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7

Cytogenetic locations: 12q21.1

OMIM:

 

613003

Gene summaries Genetic tests Medical literature

Select item 6171828.

#617182 - LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI

Cytogenetic locations: 15q21.2

OMIM:

 

617182

Gene summaries Genetic tests Medical literature

Select item 3054009.

#305400 - AARSKOG-SCOTT SYNDROME; AAS

FACIOGENITAL DYSPLASIA WITH ATTENTION DEFICIT-HYPERACTIVITY DISORDER, INCLUDED

Cytogenetic locations: Xp11.22

OMIM:

 

305400

Gene summaries Genetic tests Medical literature

Select item 14346510.

#143465 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER; ADHD

Cytogenetic locations: 1pter-p36.13, 4p16.1, 1pter-p36.13, 17p11, 1pter-p36.13, 16p13

OMIM:

 

143465

Gene summaries Genetic tests Medical literature

Select item 61745011.

#617450 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD; IDDGIP

Cytogenetic locations: 17q23.2

OMIM:

 

617450

Gene summaries Genetic tests Medical literature

Select item 13758012.

#137580 - GILLES DE LA TOURETTE SYNDROME; GTS

CHRONIC MOTOR TICS, INCLUDED

Cytogenetic locations: 15q21.2, 1pter-p36.13, 13q31.1

OMIM:

 

137580

Gene summaries Genetic tests Medical literature

Select item 24557013.

#245570 - EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION; FESD

LANDAU-KLEFFNER SYNDROME, INCLUDED; LKS, INCLUDED

Cytogenetic locations: 16p13.2

OMIM:

 

245570

Gene summaries Genetic tests Medical literature

Select item 60772114.

#607721 - NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1

Cytogenetic locations: 10q25.2

OMIM:

 

607721

Gene summaries Genetic tests Medical literature

Select item 61717315.

#617173 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA; IDDCA

Cytogenetic locations: 15q21.2

OMIM:

 

617173

Gene summaries Genetic tests Medical literature

Select item 60490616.

#604906 - SCHIZOPHRENIA 9; SCZD9

Cytogenetic locations: 1q42.2

OMIM:

 

604906

Gene summaries Genetic tests Medical literature

Select item 19068517.

#190685 - DOWN SYNDROME

DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED

Cytogenetic locations: 1pter-p36.13, 21q22.3

OMIM:

 

190685

Gene summaries Genetic tests Medical literature

Select item 20985018.

%209850 - AUTISM

AUTISM, SUSCEPTIBILITY TO, 1, INCLUDED; AUTS1, INCLUDED

Cytogenetic locations: 7q22

OMIM:

 

209850

Gene summaries Genetic tests Medical literature

Select item 60747819.

*607478 - TRYPTOPHAN HYDROXYLASE 2; TPH2

Cytogenetic locations: 12q21.1

OMIM:

 

607478

Gene summaries Genetic tests Medical literature

Select item 12645320.

+126453 - DOPAMINE RECEPTOR D5; DRD5

DYSTONIA, PRIMARY CERVICAL, INCLUDED

Cytogenetic locations: 4p16.1

OMIM:

 

126453

Gene summaries Genetic tests Medical literature