UNSW Embryology
DEVELOPMENT OF THE HEART AND CARDIOVASCULAR SYSTEM
PATENT DUCTUS ARTERIOSUS
Select Entries from OMIM |
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This page is for computers without external internet access. Normally the blue numbers below would link to a full description of the abnormality. |
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50 entries displayed (out of 71 entries found),
searching for "atrial septal defect " *600309 ATRIOVENTRICULAR SEPTAL DEFECT; AVSD *108800 ATRIAL SEPTAL DEFECT; ASD #108900 ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS *602482 AXENFELD-RIEGER ANOMALY WITH ATRIAL SEPTAL DEFECT AND SENSORINEURAL HEARING LOSS 113301 BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II 178650 PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHIC ABNORMALITIES 601927 LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND FACIAL CHANGES *220210 DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT 600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS #142900 HOLT-ORAM SYNDROME; HOS *115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A 212090 CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA *600584 CARDIAC-SPECIFIC HOMEO BOX; CSX *268310 ROBINOW SYNDROME, RECESSIVE FORM *115080 CARDIAC CONDUCTION DEFECT *100300 ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL 300166 OCULOFACIOCARDIODENTAL SYNDROME #121000 CONGENITAL HEART DISEASE *145410 HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS 147920 KABUKI SYNDROME 214800 CHOANAL ATRESIA, POSTERIOR; PCA #192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 600001 PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE *140400 HEART BLOCK #192430 VELOCARDIOFACIAL SYNDROME *255960 MYXOMA, INTRACARDIAC 270100 SITUS INVERSUS VISCERUM *263200 POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1 #200610 ACHONDROGENESIS, TYPE II; ACG2 208530 ASPLENIA WITH CARDIOVASCULAR ANOMALIES 192350 VATER ASSOCIATION 136760 FRONTONASAL DYSPLASIA 126320 DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE 224700 EBSTEIN ANOMALY #115150 CARDIOFACIOCUTANEOUS SYNDROME *225500 ELLIS-VAN CREVELD SYNDROME; EVC *241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS #153480 MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA *602730 ACTIVIN A RECEPTOR, TYPE IIB; ACVR2B 248950 MCDONOUGH SYNDROME 277200 VENTRICLE, HYPOPLASIA OF RIGHT 249670 MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION 601322 PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS 277740 WHITE FORELOCK WITH MALFORMATIONS 600987 CARDIAC MALFORMATION, CLEFT LIP-PALATE, MICROCEPHALY AND DIGITAL ANOMALIES 263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION *268300 ROBERTS SYNDROME; RBS 311900 PIERRE ROBIN SYNDROME WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT 601321 NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS 601450 DISLOCATION OF THE HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERS AND FACIAL DYSMORPHISM |
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