Epilepsy - OMIM - NCBI

Epilepsy - 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 "Epilepsy" 

267740 - RETINAL DEGENERATION AND EPILEPSY

OMIM:

 

267740

Gene summaries Genetic tests Medical literature

Select item 2268002.

226800 - EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION

OMIM:

 

226800

Gene summaries Genetic tests Medical literature

Select item 1596003.

%159600 - MYOCLONIC EPILEPSY, HARTUNG TYPE

OMIM:

 

159600

Gene summaries Genetic tests Medical literature

Select item 2268104.

226810 - EPILEPSY WITH BILATERAL OCCIPITAL CALCIFICATIONS

OMIM:

 

226810

Gene summaries Genetic tests Medical literature

Select item 2203005.

220300 - DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY

OMIM:

 

220300

Gene summaries Genetic tests Medical literature

Select item 2087006.

208700 - ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA

OMIM:

 

208700

Gene summaries Genetic tests Medical literature

Select item 6069727.

%606972 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 2; EIG2

Cytogenetic locations: 14q23

OMIM:

 

606972

Gene summaries Genetic tests Medical literature

Select item 2268508.

226850 - EPILEPSY-TELANGIECTASIA

OMIM:

 

226850

Gene summaries Genetic tests Medical literature

Select item 3103709.

310370 - MYOCLONIC EPILEPSY, PROGRESSIVE

OMIM:

 

310370

Gene summaries Genetic tests Medical literature

Select item 18261010.

182610 - SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR

OMIM:

 

182610

Gene summaries Genetic tests Medical literature

Select item 61193411.

%611934 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 5; EIG5

Cytogenetic locations: 10p11.22

OMIM:

 

611934

Gene summaries Genetic tests Medical literature

Select item 13209012.

132090 - EPILEPSY, BENIGN OCCIPITAL; BOE

OMIM:

 

132090

Gene summaries Genetic tests Medical literature

Select item 60135213.

601352 - MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE

OMIM:

 

601352

Gene summaries Genetic tests Medical literature

Select item 60957314.

%609573 - PHOTOPAROXYSMAL RESPONSE 3; PPR3

Cytogenetic locations: 7q32

OMIM:

 

609573

Gene summaries Genetic tests Medical literature

Select item 60975015.

%609750 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 4; EIG4

Cytogenetic locations: 10q25-q26

OMIM:

 

609750

Gene summaries Genetic tests Medical literature

Select item 61113616.

#611136 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13; EIG13

EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5, INCLUDED; EJM5, INCLUDED

Cytogenetic locations: 5q34

OMIM:

 

611136

Gene summaries Genetic tests Medical literature

Select item 27080517.

270805 - SPASTIC PARAPLEGIA WITH MYOCLONIC EPILEPSY

OMIM:

 

270805

Gene summaries Genetic tests Medical literature

Select item 61163018.

%611630 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3

Cytogenetic locations: 4q13.2-q21.3

OMIM:

 

611630

Gene summaries Genetic tests Medical literature

Select item 60876219.

%608762 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3; EIG3

Cytogenetic locations: 9q32-q33

OMIM:

 

608762

Gene summaries Genetic tests Medical literature

Select item 60436320.

604363 - MYOCLONIC EPILEPSY, CONGENITAL DEAFNESS, MACULAR DYSTROPHY, AND PSYCHIATRIC DISORDERS

OMIM:

 

604363

Gene summaries Genetic tests Medical literature