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Information related to Congenital cartilaginous rest of the neck

Birth defect, Congenital dermal sinus, Congenital syphilis, Congenital heart defect, Congenital melanocytic nevus, Congenital rubella syndrome, Congenital cataract, Congenital hypothyroidism, Congenital diaphragmatic hernia, Congenital insensitivity to pain, Congenital anosmia, Congenital muscular dystrophy, Congenital limb deformities, Congenital amputation, Congenital myopathy, Congenital ichthyosiform erythroderma, Congenital malaria, 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 hemolytic anemia, Congenital heart block, Congenital hypoplastic anemia, Non-progressive congenital ataxia, Congenital lip pit, Congenital fiber type disproportion, Late onset congenital adrenal hyperplasia, Congenital pulmonary airway malformation, Congenital vertebral anomaly, Congenital lactic acidosis, Congenital generalized lipodystrophy, Congenital dyserythropoietic anemia type IV, Congenital hypofibrinogenemia, Primary congenital glaucoma, Congenital blindness, Congenital contractural arachnodactyly

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

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

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