Psychiatry - OMIM - NCBI

Psychiatry - 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 "Psychiatry" 

#176200 - PORPHYRIA VARIEGATA

VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT, INCLUDED

Cytogenetic locations: 1pter-p36.13, 1q23.3

OMIM:

 

176200

Gene summaries Genetic tests Medical literature

Select item 2471002.

#247100 - LIPOID PROTEINOSIS OF URBACH AND WIETHE

Cytogenetic locations: 1q21.2

OMIM:

 

247100

Gene summaries Genetic tests Medical literature

Select item 6143323.

#614332 - CHROMOSOME 2p16.3 DELETION SYNDROME

SCHIZOPHRENIA 17, INCLUDED; SCZD17, INCLUDED

Cytogenetic locations: 2p16.3

OMIM:

 

614332

Gene summaries Genetic tests Medical literature

Select item 3098604.

*309860 - MONOAMINE OXIDASE B; MAOB

Cytogenetic locations: Xp11.3

OMIM:

 

309860

Gene summaries Genetic tests Medical literature

Select item 6005655.

*600565 - NEUREXIN I; NRXN1

Cytogenetic locations: 2p16.3

OMIM:

 

600565

Gene summaries Genetic tests Medical literature

Select item 2560006.

#256000 - LEIGH SYNDROME; LS

LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY, INCLUDED

Cytogenetic locations: 5q31.3, 1pter-p36.13, 5q11.2, 1pter-p36.13, 5p15.33, 1pter-p36.13, 2q37.3, 1pter-p36.13, 2q35, 1pter-p36.13, 19p13.3, 1pter-p36.13, 17p12, 1pter-p36.13, 12q22

OMIM:

 

256000

Gene summaries Genetic tests Medical literature

Select item 1924307.

#192430 - VELOCARDIOFACIAL SYNDROME

Cytogenetic locations: 22q11.21

OMIM:

 

192430

Gene summaries Genetic tests Medical literature

Select item 1043008.

#104300 - ALZHEIMER DISEASE; AD

ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED; AD1, INCLUDED

Cytogenetic locations: 1pter-p36.13, 6p22.2, 1pter-p36.13, 21q21.3, 1pter-p36.13, 17q22

OMIM:

 

104300

Gene summaries Genetic tests Medical literature

Select item 1815009.

#181500 - SCHIZOPHRENIA; SCZD

Cytogenetic locations: 1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q14.1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q1

OMIM:

 

181500

Gene summaries Genetic tests Medical literature

Select item 20985010.

%209850 - AUTISM

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

Cytogenetic locations: 7q22

OMIM:

 

209850

Gene summaries Genetic tests Medical literature