Congenital insensitivity to pain with partial anhidrosis

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

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