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Congenital insensitivity to pain with partial anhidrosis

Information related to Congenital insensitivity to pain with partial anhidrosis

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

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

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