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Information related to Congenital anomalies of heart

Birth defect, Congenital dermal sinus, Congenital syphilis, Congenital heart defect, Congenital melanocytic nevus, Congenital rubella syndrome, Congenital diaphragmatic hernia, Congenital cataract, Congenital hypothyroidism, Congenital insensitivity to pain, Congenital anosmia, Congenital muscular dystrophy, Congenital limb deformities, Congenital ichthyosiform erythroderma, Congenital myopathy, Congenital malaria, Congenital amputation, Congenital dyserythropoietic anemia, Congenital adrenal hyperplasia, Congenital absence of the vas deferens, Severe congenital neutropenia, Congenital chloride diarrhea, Congenital myasthenic syndrome, Congenital nephrotic syndrome, Leber congenital amaurosis, Congenital heart block, Congenital hemolytic anemia, Congenital hypoplastic anemia, Congenital lip pit, Late onset congenital adrenal hyperplasia, Non-progressive congenital ataxia, Congenital fiber type disproportion, Congenital pulmonary airway malformation, Congenital vertebral anomaly, Congenital lactic acidosis, Congenital generalized lipodystrophy, Congenital hypofibrinogenemia, Primary congenital glaucoma, Congenital blindness, Congenital dyserythropoietic anemia type IV, Congenital iodine deficiency syndrome

Congenital contractural arachnodactyly, Congenital stationary night blindness, Congenital portosystemic shunt, List of ICD-9 codes 740–759: congenital anomalies, Ullrich congenital muscular dystrophy, Congenital onychodysplasia of the index fingers, Congenital hereditary endothelial dystrophy, Congenital fourth nerve palsy, Congenital hyperinsulinism, Fukuyama congenital muscular dystrophy, Congenital distal spinal muscular atrophy, Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome, Congenital stromal corneal dystrophy, Congenital cartilaginous rest of the neck, Congenital epulis, Congenital dyserythropoietic anemia type III, Congenital dyserythropoietic anemia type I, Lethal congenital contracture syndrome, Distichiasis, congenital heart defects and mixed peripheral vascular anomalies, Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency, Congenital disorder of glycosylation, Congenital dyserythropoietic anemia type II, Congenital varicella syndrome, Congenital athymia, Congenital red–green color blindness, Isolated congenital asplenia, Congenital afibrinogenemia, Congenital clasped thumb, LMNA-related congenital muscular dystrophy, World Journal for Pediatric and Congenital Heart Surgery, Congenital hepatic fibrosis, List of congenital disorders, Congenital erosive and vesicular dermatosis, Congenital amegakaryocytic thrombocytopenia, Late congenital syphilitic oculopathy, Congenital stenosis of vena cava, Congenital smooth muscle hamartoma, Congenital pseudarthrosis of the tibia, Congenital trigger thumb, Congenital Heart Surgeons' Society, Aplasia cutis congenita, Congenital cytomegalovirus infection, Hypomyelination-congenital cataract syndrome, Cystic eyeball, Compton-North congenital myopathy, Gunther disease, Vascular tumor, Congenital tufting enteropathy, Megaureter, LAMA2 related congenital muscular dystrophy

Birth defect, Congenital dermal sinus, Congenital syphilis, Congenital heart defect, Congenital melanocytic nevus, Congenital rubella syndrome, Congenital diaphragmatic hernia, Congenital cataract, Congenital hypothyroidism, Congenital insensitivity to pain, Congenital anosmia, Congenital muscular dystrophy, Congenital limb deformities, Congenital ichthyosiform erythroderma, Congenital myopathy, Congenital malaria, Congenital amputation, Congenital dyserythropoietic anemia, Congenital adrenal hyperplasia, Congenital absence of the vas deferens, Severe congenital neutropenia, Congenital chloride diarrhea, Congenital myasthenic syndrome, Congenital nephrotic syndrome, Leber congenital amaurosis, Congenital heart block, Congenital hemolytic anemia, Congenital hypoplastic anemia, Congenital lip pit, Late onset congenital adrenal hyperplasia, Non-progressive congenital ataxia, Congenital fiber type disproportion, Congenital pulmonary airway malformation, Congenital vertebral anomaly, Congenital lactic acidosis, Congenital generalized lipodystrophy, Congenital hypofibrinogenemia, Primary congenital glaucoma, Congenital blindness, Congenital dyserythropoietic anemia type IV, Congenital iodine deficiency syndrome, Congenital contractural arachnodactyly, Congenital stationary night blindness, Congenital portosystemic shunt, List of ICD-9 codes 740–759: congenital anomalies, Ullrich congenital muscular dystrophy, Congenital onychodysplasia of the index fingers, Congenital hereditary endothelial dystrophy, Congenital fourth nerve palsy, Congenital hyperinsulinism, Fukuyama congenital muscular dystrophy, Congenital distal spinal muscular atrophy, Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome, Congenital stromal corneal dystrophy, Congenital cartilaginous rest of the neck, Congenital epulis, Congenital dyserythropoietic anemia type III, Congenital dyserythropoietic anemia type I, Lethal congenital contracture syndrome, Distichiasis, congenital heart defects and mixed peripheral vascular anomalies, Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency, Congenital disorder of glycosylation, Congenital dyserythropoietic anemia type II, Congenital varicella syndrome, Congenital athymia, Congenital red–green color blindness, Isolated congenital asplenia, Congenital afibrinogenemia, Congenital clasped thumb, LMNA-related congenital muscular dystrophy, World Journal for Pediatric and Congenital Heart Surgery, Congenital hepatic fibrosis, List of congenital disorders, Congenital erosive and vesicular dermatosis, Congenital amegakaryocytic thrombocytopenia, Late congenital syphilitic oculopathy, Congenital stenosis of vena cava, Congenital smooth muscle hamartoma, Congenital pseudarthrosis of the tibia, Congenital trigger thumb, Congenital Heart Surgeons' Society, Aplasia cutis congenita, Congenital cytomegalovirus infection, Hypomyelination-congenital cataract syndrome, Cystic eyeball, Compton-North congenital myopathy, Gunther disease, Vascular tumor, Congenital tufting enteropathy, Megaureter, LAMA2 related congenital muscular dystrophy, Congenital fibrosis of the extraocular muscles, Absence of fingerprints-congenital milia syndrome, Rocker bottom foot, Congenital insensitivity to pain with anhidrosis, Congenital disorder of glycosylation type IIc, Congenital mirror movement disorder, Fibular hemimelia, Cutis marmorata telangiectatica congenita, Mesoblastic nephroma, Microcoria, Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency, Multiple congenital anomalies-hypotonia-seizures syndrome, Amaurosis congenita, cone-rod type, with congenital hypertrichosis, Multiple abnormalities, Lipoid congenital adrenal hyperplasia, Hypertrichosis 1 (universalis, congenital), Congenital hearing loss, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Preauricular sinus and cyst, Congenital Agenesis of Gender Ideation, Nasolacrimal duct obstruction, Congenital malformations of the dermatoglyphs, Congenital bilateral perisylvian syndrome, Constriction ring syndrome, Urinary tract obstruction, Congenital contractural arachnodactyly in cattle, Zonular cataract and nystagmus, X-linked hypertrichosis, Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency, Congenital cutaneous candidiasis, Hip dysplasia, Congenital self-healing reticulohistiocytosis, Central hypoventilation syndrome, National Congenital Heart Disease Audit, Sucrose intolerance, Hypertrichosis, Isolated hypogonadotropic hypogonadism, Alveolar capillary dysplasia, CHILD syndrome, Bruck syndrome, Cataract-microcornea syndrome, Kindler syndrome, PMM2 deficiency, Elimination Initiative, Infantile esotropia, Congenital sensorineural deafness in cats, Congenital hypertrophy of the retinal pigment epithelium, Congenital hypertrophy of the lateral fold of the hallux, Factor X deficiency, Hypotonia, Proximal femoral focal deficiency, Rubella, Toxoplasmosis, Posterior urethral valve, Nystagmus, PELVIS syndrome, Worster-Drought syndrome, Amusia, Epidermolytic hyperkeratosis, Ichthyosis with confetti

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