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Information related to Congenital contractural arachnodactyly

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

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

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

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