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