Congenital insensitivity to pain with partial anhidrosis

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

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

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