Heart And Vascular Diseases - OMIM - NCBI

Heart And Vascular Diseases - OMIM - NCBI

1.

*102620 - ACTIN, ALPHA-2, SMOOTH MUSCLE, AORTA; ACTA2

Cytogenetic locations: 10q23.31

OMIM:

 

102620

Gene summaries Genetic tests Medical literature

Select item 1363522.

*136352 - FMS-LIKE TYROSINE KINASE 4; FLT4

Cytogenetic locations: 5q35.3

OMIM:

 

136352

Gene summaries Genetic tests Medical literature

Select item 1922403.

*192240 - VASCULAR ENDOTHELIAL GROWTH FACTOR A; VEGFA

Cytogenetic locations: 6p21.1

OMIM:

 

192240

Gene summaries Genetic tests Medical literature

Select item 3001664.

#300166 - MICROPHTHALMIA, SYNDROMIC 2; MCOPS2

Cytogenetic locations: Xp11.4

OMIM:

 

300166

Gene summaries Genetic tests Medical literature

Select item 6111395.

%611139 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 8; CHDS8

Cytogenetic locations: 9p21

OMIM:

 

611139

Gene summaries Genetic tests Medical literature

Select item 1096306.

+109630 - BETA-1-ADRENERGIC RECEPTOR; ADRB1

CONGESTIVE HEART FAILURE AND BETA-BLOCKER RESPONSE, MODIFIER OF, INCLUDED

Cytogenetic locations: 10q25.3

OMIM:

 

109630

Gene summaries Genetic tests Medical literature

Select item 6091927.

#609192 - LOEYS-DIETZ SYNDROME 1; LDS1

Cytogenetic locations: 9q22.33

OMIM:

 

609192

Gene summaries Genetic tests Medical literature

Select item 2599008.

#259900 - HYPEROXALURIA, PRIMARY, TYPE I; HP1

Cytogenetic locations: 2q37.3

OMIM:

 

259900

Gene summaries Genetic tests Medical literature

Select item 1547009.

#154700 - MARFAN SYNDROME; MFS

Cytogenetic locations: 15q21.1

OMIM:

 

154700

Gene summaries Genetic tests Medical literature

Select item 19405010.

#194050 - WILLIAMS-BEUREN SYNDROME; WBS

Cytogenetic locations: 7q11.23

OMIM:

 

194050

Gene summaries Genetic tests Medical literature

Select item 23230011.

#232300 - GLYCOGEN STORAGE DISEASE II; GSD2

Cytogenetic locations: 17q25.3

OMIM:

 

232300

Gene summaries Genetic tests Medical literature

Select item 30150012.

#301500 - FABRY DISEASE

FABRY DISEASE, CARDIAC VARIANT, INCLUDED

Cytogenetic locations: Xq22.1

OMIM:

 

301500

Gene summaries Genetic tests Medical literature

Select item 12552013.

%125520 - CAYLER CARDIOFACIAL SYNDROME

Cytogenetic locations: 22q11

OMIM:

 

125520

Gene summaries Genetic tests Medical literature

Select item 18840014.

#188400 - DIGEORGE SYNDROME; DGS

DIGEORGE SYNDROME CHROMOSOME REGION, INCLUDED; DGCR, INCLUDED

Cytogenetic locations: 22q11.21

OMIM:

 

188400

Gene summaries Genetic tests Medical literature

Select item 61016815.

#610168 - LOEYS-DIETZ SYNDROME 2; LDS2

Cytogenetic locations: 3p24.1

OMIM:

 

610168

Gene summaries Genetic tests Medical literature

Select item 13921016.

#139210 - MYHRE SYNDROME; MYHRS

Cytogenetic locations: 18q21.2

OMIM:

 

139210

Gene summaries Genetic tests Medical literature

Select item 17390017.

#173900 - POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD1

Cytogenetic locations: 16p13.3

OMIM:

 

173900

Gene summaries Genetic tests Medical literature

Select item 18084918.

#180849 - RUBINSTEIN-TAYBI SYNDROME 1; RSTS1

Cytogenetic locations: 16p13.3

OMIM:

 

180849

Gene summaries Genetic tests Medical literature

Select item 53500019.

#535000 - LEBER OPTIC ATROPHY

OMIM:

 

535000

Gene summaries Genetic tests Medical literature

Select item 24515020.

#245150 - KEUTEL SYNDROME; KTLS

Cytogenetic locations: 12p12.3

OMIM:

 

245150

Gene summaries Genetic tests Medical literature