ACED |
anhidrotic congenital ectodermal dysplasia |
|
CAD |
Congenital Abduction Deficiency |
|
CAH |
Congenital Adrenal Hyperplasia |
|
CALP |
Congenital Absence of Left Pericardium |
|
CAMV |
congenital anomaly of mitral valve |
|
CAR |
Congenital Articular Rigidity |
|
CAS |
congenital alcoholic syndrome |
|
CASMD |
Congenital Atonic Sclerotic Muscular Dystrophy |
|
cAV |
Congenital Adrenal Virilism |
|
cAV |
Congenital Absence of Vagina |
|
cavd |
congenital aplasia of vas deferens |
|
CBAVD |
Congenital Bilateral Absence Of Vas Deferens |
|
CBPS |
Chemical And Biological Protected Shelter |
|
CBPS |
Congenital Bilateral Perisylvian Syndrome |
|
CC-TGA |
Congenitally Corrected Transposition Of Great Vessels |
|
CCA |
Congenital Contractural Arachnodactyly |
|
CCAM |
Classification Commune des Actes Medicaux |
|
CCAM |
Congenital Cystic Adenomatoid Malformation |
|
CCHD |
Cyanotic Congenital Heart Disease |
|
CCHD |
Caephilly Collaborative Heart Disease |
|
CCHS |
Congenital central hypoventilation syndrome |
|
CCHS |
Copenhagen City Heart Study |
|
CCVM |
congenital cardiovascular malformation |
|
cda |
congenital dyserythropoietic anemia |
|
cdd |
congenital diaphragmatic defect |
|
CDG |
Congenital Disorders Of Glycosylation |
|
CDO |
Congenital duodenal obstruction |
|
CEP |
Congenital Erythropoietic Porphyria |
|
CET |
Congenital Eyelid Tetrad |
|
CEU |
Congenital ectropion uveae |
|
CEU |
Continuing Education Unit |
|
CGAB |
Congenital Abnormality |
|
CGFH |
Congenital Fibrous Histiocytoma |
|
CH |
congenital hypothyroidism |
|
CHA |
Congenital Hypoplastic Anemia |
|
CHB |
Chronic Hepatitis B |
|
CHBA |
Congenital Heinz Body Hemolytic Anemia |
|
CHBHA |
Congenital Heinz Body Hemolytic Anemia |
|
CHCL |
Congenital Healed Cleft Lip |
|
CHD |
Congenital Heart Disease |
|
CHD |
Congenital Hip Dislocation |
|
CHED |
Congenital Heredity Endothelial Dystrophy |
|
CHF |
Congenital Hepatic Fibrosis |
|
CHHS |
congenital hypothalamic hamartoma syndrome |
|
CHILD |
congenital hemidysplasia with ichthyosiform erythroderma and limb defects |
|
CHILD SYNDROME |
Congenital Hemidysplasia With Ichthyosiform Erythrodermal And Limb Defects |
|
CHRPE |
Congenital Hypertrophy of the Retinal Pigment Epithelium |
|
CHS |
Congenital Heart Surgeons Society study |
|
CHS |
congenital hypoventilation syndrome |
|
CIA |
Colony-inhibiting Activity |
|
CIA |
Congenital Intestinal Aganglionosis |
|
CIBHA |
Congenital Inclusion-body Hemolytic Anemia |
|
CIE |
Congenital Ichthyosiform Erythroderma |
|
CLAH |
Congenital Lipoid Adrenal Hyperplasia |
|
CLAS |
Congenital Localized Absence of Skin |
|
CLD |
Congenital Limb Deficiency |
|
Cm |
Congenital Malformation |
|
CMD |
Congenital Muscular Dystrophy |
|
CMH |
Community Mental Health |
|
CMH |
Congenital Malformation of the Heart |
|
CMR |
congenital mitral regurgitation |
|
CMSD |
congenital myocardial sympathetic dysinnervation |
|
CN |
Congenital Nystagmus |
|
CNDI |
Congenital Nephrogenic Diabetes Insipidus |
|
CNF |
Congenital Nephrotic Syndrome Of The Finnish |
|
CNHD |
Congenital Nonspherocytic Hemolytic Disease |
|
CNS |
Congenital Nephrotic Syndrome |
|
CNSHA |
Congenital Nonspherocytic Hemolytic Anemia |
|
COACH |
Canadian Organization for the Advancement of Computers in Healthcare |
|
COIF |
Congenital Onychodysplasia of the Index Finger |
|
congen |
congenital |
|
CONGHD |
Congenital Heart Disease |
|
CPCL |
congenital pulmonary cystic lymphangiectasia |
|
CPD |
Childhood Or Congenital Polycystic Disease |
|
CPI |
congenital palatopharyngeal incompetence |
|
CPL |
Congenital Pulmonary Lymphangiectasia |
|
CPVD |
Congenital Polyvalvular Disease |
|
CRB |
congenital retinal blindness |
|
CRD |
congenital rubella deafness |
|
CRI |
Congenital Rubella Infection |
|
CROME |
Congenital Cataracts-epileptic Fits-mental Retardation |
|
CRS |
Congenital Rubella Syndrome |
|
CS |
Congenital Syphilis |
|
CSB |
congenital short bowel |
|
CSHH |
Congenital Self-Healing Histiocytosis |
|
CSHRH |
Congenital Self-healing Reticulohistiocytosis |
|
CSNA |
congenital sensory neuropathy with anhidrosis |
|
CSNB |
Congenital Stationary Night Blindness |
|
CTA |
congenital trigeminal anesthesia |
|
CTD |
Congenital Thymic Dysplasia |
|
ctev |
congenital talipes equinovarus |
|
CUAVD |
Congenital Unilateral Absence of Vas Deferens |
|
CVAH |
Congenital Virilizing Adrenal Hyperplasia |
|
CVBS |
congenital vascular bone syndrome |
|
CVD |
congenital vascular disorder |
|
CVM |
Congenital Vascular Malformation |
|
CVT |
central venous temperature |
|
CVT |
Cerebral Venous Thrombosis |
|
EUROHAZCON |
Congenital Anomalies Near Hazardous Waste Landfill Sites In Europe |
|
FCCA |
familial congenital cardiac abnormality |
|
FCMD |
Fukuyama Congenital Muscular Dystrophy |
|
HIPO |
Hospital Indicator for Physicians Orders |
|
HYCX |
Hydrocephalus Due To Congenital Stenosis Of Aqueduct Of Sylvius |
|
LCA |
Leber congenital amaurosis |
|
LCAH |
Lipoid Congenital Adrenal Hyperplasia |
|
LCB |
Leber congenital blindness |
|
LCB |
Laboratory of Cancer Biology |
|
LCSS |
Lethal Congenital Contracture Syndrome |
|
MACDP |
Metropolitan Atlanta Congenital Defects Program |
|
MCA |
Multiple Congenital Anomaly |
|
Mca/mr |
Multiple Congenital Anomaly/Mental Retardation |
|
NCRSP |
National Congenital Rubella Surveillance Programme |
|
NHS-1 |
First Natural History Study |
|
NHS-2 |
Second Natural History Study |
|
SCA |
Severe Congenital Anomaly |
|
TORCH |
Congenital Infections: T = Toxoplasmosis |
|
TORCH |
Toxoplasmosis, Other, Rubella, Cytomegalovirus, And Herpes Simplex Virus |
|
U |
Congenital Limb Absence |
|
VACA |
Valvuloplasty and Angioplasty in Congenital Anomalies |
|
VINDICATE |
Vascular, Inflammatory, Neoplastic, Degenerative, Intoxication, Congenital, Allergic, Trauma, Endocrine |
|