UNSW Embryology
DEVELOPMENT OF THE HEART AND CARDIOVASCULAR SYSTEM
TETRALOGY OF FALLOT
Select Entries from OMIM |
|
|
This page is for computers without external internet access. Normally the blue numbers below would link to a full description of the abnormality. |
|
|
38 entries found, searching for "tetralogy of
fallot" 187500 TETRALOGY OF FALLOT 239711 HYPERTELORISM AND TETRALOGY OF FALLOT 187501 TETRALOGY OF FALLOT AND GLAUCOMA 601127 FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION *188400 DIGEORGE SYNDROME; DGS #192430 VELOCARDIOFACIAL SYNDROME #179613 RECOMBINANT CHROMOSOME 8 SYNDROME 217095 CONOTRUNCAL HEART MALFORMATIONS; CTHM *163950 NOONAN SYNDROME 1; NS1 #115470 CAT EYE SYNDROME; CES *134820 FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA 136760 FRONTONASAL DYSPLASIA 601348 ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA 147920 KABUKI SYNDROME *107600 APLASIA CUTIS CONGENITA *250620 METHACRYLICACIDURIA *211750 C SYNDROME 154400 ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 #270400 SMITH-LEMLI-OPITZ SYNDROME, TYPE I *274000 THROMBOCYTOPENIA--ABSENT RADIUS SYNDROME *145410 HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS *125520 DEPRESSOR ANGULI ORIS MUSCLE, HYPOPLASIA OF #118450 ALAGILLE SYNDROME; AGS 214800 CHOANAL ATRESIA, POSTERIOR; PCA 280000 ZUNICH NEUROECTODERMAL SYNDROME 309350 MELNICK-NEEDLES OSTEODYSPLASTY 600001 PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE *600309 ATRIOVENTRICULAR SEPTAL DEFECT; AVSD *600584 CARDIAC-SPECIFIC HOMEO BOX; CSX 227255 FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS *162660 NEUROTROPHIN 3; NTF3 600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS *216340 CLEIDOCRANIAL DYSPLASIA WITH MICROGNATHIA, ABSENT THUMBS, AND DISTAL APHALANGIA 601322 PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS *601920 JAGGED 1; JAG1 166780 OTOFACIOCERVICAL SYNDROME 602249 PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES 603530 LIGHT FIXATION SEIZURE SYNDROME |
|