Stroke - OMIM - NCBI

Stroke - 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 "Stroke" 

%606799 - STROKE, SUSCEPTIBILITY TO, 1

Cytogenetic locations: 5q11.2-q12.1

OMIM:

 

606799

Gene summaries Genetic tests Medical literature

Select item 6145192.

#614519 - HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO; ICH

Cytogenetic locations: 13q34, 1pter-p36.13, 13q34

OMIM:

 

614519

Gene summaries Genetic tests Medical literature

Select item 6013673.

#601367 - STROKE, ISCHEMIC

Cytogenetic locations: 1q24.2, 1pter-p36.13, 14q23.1, 1pter-p36.13, 13q12.3

OMIM:

 

601367

Gene summaries Genetic tests Medical literature

Select item 5400004.

#540000 - MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS

OMIM:

 

540000

Gene summaries Genetic tests Medical literature

Select item 1256355.

125635 - DERMOGRAPHISM, FAMILIAL

OMIM:

 

125635

Gene summaries Genetic tests Medical literature

Select item 1637296.

+163729 - NITRIC OXIDE SYNTHASE 3; NOS3

CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 7q36.1

OMIM:

 

163729

Gene summaries Genetic tests Medical literature

Select item 6156887.

#615688 - POLYARTERITIS NODOSA, CHILDHOOD-ONSET; PAN

Cytogenetic locations: 22q11.1

OMIM:

 

615688

Gene summaries Genetic tests Medical literature

Select item 6037008.

*603700 - ARACHIDONATE 5-LIPOXYGENASE-ACTIVATING PROTEIN; ALOX5AP

Cytogenetic locations: 13q12.3

OMIM:

 

603700

Gene summaries Genetic tests Medical literature

Select item 1923159.

#192315 - VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL

Cytogenetic locations: 3p21.31

OMIM:

 

192315

Gene summaries Genetic tests Medical literature

Select item 20805010.

#208050 - ARTERIAL TORTUOSITY SYNDROME; ATS

Cytogenetic locations: 20q13.12

OMIM:

 

208050

Gene summaries Genetic tests Medical literature

Select item 60012911.

*600129 - PHOSPHODIESTERASE 4D, cAMP-SPECIFIC; PDE4D

Cytogenetic locations: 5q11.2-q12.1

OMIM:

 

600129

Gene summaries Genetic tests Medical literature

Select item 60605412.

#606054 - PROPIONIC ACIDEMIA

Cytogenetic locations: 1pter-p36.13, 13q32.3

OMIM:

 

606054

Gene summaries Genetic tests Medical literature

Select item 23730013.

#237300 - CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO

Cytogenetic locations: 2q34

OMIM:

 

237300

Gene summaries Genetic tests Medical literature

Select item 25100014.

#251000 - METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY

METHYLMALONIC ACIDURIA, mut(0) TYPE, INCLUDED

Cytogenetic locations: 6p12.3

OMIM:

 

251000

Gene summaries Genetic tests Medical literature

Select item 24927015.

#249270 - THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA

Cytogenetic locations: 1q24.2

OMIM:

 

249270

Gene summaries Genetic tests Medical literature

Select item 13558016.

135580 - FIBROMUSCULAR DYSPLASIA; FMDA

OMIM:

 

135580

Gene summaries Genetic tests Medical literature

Select item 21570017.

#215700 - CITRULLINEMIA, CLASSIC

Cytogenetic locations: 9q34.11

OMIM:

 

215700

Gene summaries Genetic tests Medical literature

Select item 17578018.

#175780 - PORENCEPHALY 1; POREN1

Cytogenetic locations: 13q34

OMIM:

 

175780

Gene summaries Genetic tests Medical literature

Select item 61677919.

#616779 - CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2

Cytogenetic locations: 10q26.13

OMIM:

 

616779

Gene summaries Genetic tests Medical literature

Select item 60390320.

#603903 - SICKLE CELL ANEMIA

Cytogenetic locations: 11p15.4

OMIM:

 

603903

Gene summaries Genetic tests Medical literature