UNSW Embryology
DEVELOPMENT OF THE HEART AND CARDIOVASCULAR SYSTEM
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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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100 entries displayed (out of 879 entries found), searching for "heart" |
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*113900 BUNDLE BRANCH BLOCK (Click here to see a typical entry, no external links will work from this page.) 261740 PHOSPHORYLASE KINASE DEFICIENCY OF HEART 234700 HEART BLOCK, CONGENITAL *140400 HEART BLOCK *121014 GAP JUNCTION PROTEIN, ALPHA-1, 43-KD; GJA1 #121000 CONGENITAL HEART DISEASE #142900 HOLT-ORAM SYNDROME; HOS 232330 GLYCOGEN STORAGE DISEASE IIb *236700 MCKUSICK-KAUFMAN SYNDROME; MKKS *134651 FATTY ACID-BINDING PROTEIN 3, MUSCLE AND HEART; FABP3 214800 CHOANAL ATRESIA, POSTERIOR; PCA 140500 HEART, MALFORMATION OF 217095 CONOTRUNCAL HEART MALFORMATIONS; CTHM *314400 CARDIAC VALVULAR DYSPLASIA, X-LINKED 241550 HYPOPLASTIC LEFT HEART SYNDROME *118938 CHYMASE, HEART; CYH 601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE *123875 CYSTEINE-RICH INTESTINAL PROTEIN 1; CRIP1 601348 ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA 218450 CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS #220400 JERVELL AND LANGE-NIELSEN SYNDROME 300166 OCULOFACIOCARDIODENTAL SYNDROME 126190 DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS 600001 PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE 244300 KAPUR-TORIELLO SYNDROME 270460 SONODA SYNDROME 126320 DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE *600378 HEART MUSCLE PROTEIN; HMP 217085 CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY 108770 ATRIAL CARDIOMYOPATHY WITH HEART BLOCK 140450 HEART-HAND SYNDROME, SPANISH TYPE *249620 MENTAL RETARDATION, CONGENITAL HEART DISEASE, BLEPHAROPHIMOSIS, BLEPHAROPTOSIS, AND HYPOPLASTIC TEETH *602915 TRYPTOPHAN-RICH BASIC PROTEIN; WRB 246570 LIMB DEFICIENCY-HEART MALFORMATION SYNDROME 601355 MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS, AND HYPOSEGMENTED LUNGS 311900 PIERRE ROBIN SYNDROME WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT 245210 KOUSSEFF SYNDROME 602531 ARTERIAL OCCLUSIVE DISEASE, PROGRESSIVE, WITH HYPERTENSION, HEART DEFECTS, BONE FRAGILITY, AND BRACHYSYNDACTYLY *601364 CADHERIN 13; CDH13 *602988 PROTOCADHERIN 7; PCDH7 215850 CLEFT-LIMB-HEART MALFORMATION SYNDROME 234750 HEART, MALFORMATION OF *600309 ATRIOVENTRICULAR SEPTAL DEFECT; AVSD *176300 TRANSTHYRETIN; TTR *310200 MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES *188400 DIGEORGE SYNDROME; DGS *600584 CARDIAC-SPECIFIC HOMEO BOX; CSX *192500 LONG QT SYNDROME, TYPE 1 *106180 DIPEPTIDYL CARBOXYPEPTIDASE 1; DCP1 *143890 HYPERCHOLESTEROLEMIA, FAMILIAL; FHC *310300 EMERY-DREIFUSS MUSCULAR DYSTROPHY #530000 KEARNS-SAYRE SYNDROME; KSS 270100 SITUS INVERSUS VISCERUM *103220 ADENINE NUCLEOTIDE TRANSLOCATOR 1; ANT1 #108900 ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS *107741 APOLIPOPROTEIN E; APOE *244400 KARTAGENER SYNDROME *102540 ACTIN, ALPHA, CARDIAC MUSCLE; ACTC *107600 APLASIA CUTIS CONGENITA *160900 DYSTROPHIA MYOTONICA; DMPK #192430 VELOCARDIOFACIAL SYNDROME *600576 GATA-BINDING PROTEIN 4; GATA4 *160710 MYOSIN, HEAVY POLYPEPTIDE 6; MYH6 *191045 TROPONIN T2, CARDIAC; TNNT2 #192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 *106165 ANGIOTENSIN RECEPTOR 1; AGTR1 *220210 DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT #190685 TRISOMY 21 *600857 SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN; SDHA *231050 GELEOPHYSIC DYSPLASIA #118450 ALAGILLE SYNDROME; AGS 602941 CRK-ASSOCIATED SUBSTRATE *600295 NATRIURETIC PEPTIDE PRECURSOR B; NPPB *120220 COLLAGEN, TYPE VI, ALPHA-1; COL6A1 *106700 TOTAL ANOMALOUS PULMONARY VENOUS RETURN; TAPVR1 *117550 CEREBRAL GIGANTISM *302060 BARTH SYNDROME; BTHS *115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A *160760 MYOSIN, CARDIAC, HEAVY CHAIN, BETA; MYH7 236110 HOLZGREVE SYNDROME 120000 COARCTATION OF AORTA *107730 APOLIPOPROTEIN B; APOB *602406 HLH TRANSCRIPTION FACTOR HAND1 *238600 HYPERLIPOPROTEINEMIA, TYPE I #268670 RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROME #118200 CHARCOT-MARIE-TOOTH DISEASE 1B; CMT1B *600438 TRANSCRIPTION FACTOR A, MITOCHONDRIAL; TFAM *259900 OXALOSIS I 208530 ASPLENIA WITH CARDIOVASCULAR ANOMALIES *601609 L-3-@HYDROXYACYL-CoA DEHYDROGENASE, SHORT CHAIN; HADHSC *600884 CARDIOMYOPATHY, DILATED, 1B; CMD1B *602694 NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 4; NDUFS4 #115470 CAT EYE SYNDROME; CES *602447 PARAOXONASE 2; PON2 *602538 RNA-BINDING PROTEIN ETR3 #231005 GAUCHER-LIKE DISEASE *261600 PHENYLKETONURIA; PKU1 264480 PSEUDOTRISOMY 13 SYNDROME *236200 HOMOCYSTINURIA *235200 HEMOCHROMATOSIS; HFE |
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