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All: 198 
OMIM dbSNP: 14 
OMIM UniSTS: 47 
Items 1 - 20 of 198
 
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1: #600309 Links
ATRIOVENTRICULAR SEPTAL DEFECT; AVSD
ATRIOVENTRICULAR CANAL DEFECT; AVCD
Gene map locus 6q21-q23.2, 1p31-p21
2: 178370 Links
PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT
3: #113900 GeneTests, Links
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE I; PFHBI
HEART BLOCK, NONPROGRESSIVE, INCLUDED
Gene map locus 19q13.2-q13.3, 3p21
4: 235750 Links
HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT
5: 600123 Links
ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS
6: #192600 GeneTests, Links
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC; CMH
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1, INCLUDED; CMH1, INCLUDED
Gene map locus 20q13.3, 15q14, 14q12, 14q12, 3p21.3-p14.3, 3p25
7: %220210 Links
DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT
8: %107600 GeneTests, Links
APLASIA CUTIS CONGENITA
9: #108900 GeneTests, Links
ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS
Gene map locus 5q34
10: +160710 Links
MYOSIN, HEAVY CHAIN 6, CARDIAC MUSCLE, ALPHA; MYH6
ATRIAL SEPTAL DEFECT 3, INCLUDED; ASD3, INCLUDED
Gene map locus 14q12
11: #607941 Links
ATRIAL SEPTAL DEFECT 2; ASD2
Gene map locus 8p23.1-p22
12: 602561 Links
BRACHYDACTYLY, INTRAVENTRICULAR SEPTAL DEFECT, AND DEAFNESS
13: #300166 GeneTests, Links
MICROPHTHALMIA, SYNDROMIC 2; MCOPS2
Gene map locus Xp11.4
14: 212090 Links
CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA
15: #115200 GeneTests, Links
CARDIOMYOPATHY, DILATED, 1A; CMD1A
Gene map locus 1q21.2, 11p11.2
16: #192500 GeneTests, Links
LONG QT SYNDROME 1; LQT1
Gene map locus 11p15.5
17: *602937 Links
CBP/p300-INTERACTING TRANSACTIVATOR, WITH GLU/ASP-RICH C-TERMINAL DOMAIN, 2; CITED2
CARDIAC SEPTAL DEFECTS, INCLUDED
Gene map locus 6q23.3
18: 270460 Links
SONODA SYNDROME
19: 231060 Links
GENITOPALATOCARDIAC SYNDROME
20: 601348 Links
ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA
Items 1 - 20 of 198
 
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