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Metadata
ID	HP:0001197
Name	Abnormality of prenatal development or birth
Parent Relationships	is_a Phenotypic abnormality
Related Diseases	disease has basis in congenital hypothyroidism early congenital syphilis congenital stationary night blindness congenital adrenal insufficiency congenital muscular dystrophy Ullrich congenital muscular dystrophy Fukuyama congenital muscular dystrophy congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital generalized lipodystrophy severe congenital neutropenia primary congenital glaucoma congenital bile acid synthesis defect congenital intrinsic factor deficiency congenital adrenal hyperplasia spondyloepiphyseal dysplasia with congenital joint dislocations congenital ptosis congenital secretory chloride diarrhea 1 congenital stromal corneal dystrophy lethal congenital contracture syndrome lethal congenital contracture syndrome 1 lethal congenital contracture syndrome 2 neonatal diabetes mellitus with congenital hypothyroidism congenital chylothorax congenital hereditary endothelial dystrophy of cornea lethal congenital contracture syndrome 3 lethal congenital contracture syndrome 4 autosomal recessive congenital ichthyosis autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 4B autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 11 congenital central hypoventilation syndrome T-cell immunodeficiency, congenital alopecia, and nail dystrophy congenital diarrhea congenital diarrhea 5 with tufting enteropathy congenital secretory sodium diarrhea 8 congenital diarrhea 7 with exudative enteropathy congenital malabsorptive diarrhea 4 congenital diarrhea 6 congenital secretory sodium diarrhea 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 6 congenital disorder of glycosylation type IIa congenital disorder of glycosylation type IIb congenital disorder of glycosylation type IIc congenital disorder of glycosylation type IId congenital disorder of glycosylation type IIe congenital disorder of glycosylation type IIf congenital disorder of glycosylation type IIg congenital disorder of glycosylation type IIh congenital disorder of glycosylation type IIi congenital disorder of glycosylation type IIj congenital disorder of glycosylation type IIk congenital disorder of glycosylation type IIl congenital disorder of glycosylation type IIm congenital disorder of glycosylation type IIn congenital disorder of glycosylation type IIo congenital disorder of glycosylation type IIp congenital disorder of glycosylation type IIq physical disorder nonsyndromic congenital nail disorder 1 nonsyndromic congenital nail disorder 2 nonsyndromic congenital nail disorder 3 nonsyndromic congenital nail disorder 4 nonsyndromic congenital nail disorder 5 nonsyndromic congenital nail disorder 6 nonsyndromic congenital nail disorder 7 nonsyndromic congenital nail disorder 8 nonsyndromic congenital nail disorder 9 Compton-North congenital myopathy congenital myopathy 4A multiple congenital anomalies-hypotonia-seizures syndrome 1 multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple congenital anomalies-hypotonia-seizures syndrome 3 congenital fibrosis of the extraocular muscles Zika virus congenital syndrome congenital muscular dystrophy with cataracts and intellectual disability autosomal recessive congenital ichthyosis 13 autosomal recessive congenital ichthyosis 14 multiple congenital anomalies-hypotonia-seizures syndrome congenital disorder of glycosylation Ia congenital disorder of glycosylation Iaa congenital disorder of glycosylation Ib congenital disorder of glycosylation Ic congenital disorder of glycosylation Id congenital disorder of glycosylation Ie congenital disorder of glycosylation If congenital disorder of glycosylation Ig congenital disorder of glycosylation Ih congenital disorder of glycosylation Ii congenital disorder of glycosylation Ij congenital disorder of glycosylation Ik congenital disorder of glycosylation Il congenital disorder of glycosylation Im congenital disorder of glycosylation In congenital disorder of glycosylation Ip congenital disorder of glycosylation Iq congenital disorder of glycosylation Ir congenital disorder of glycosylation It congenital disorder of glycosylation Iu congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix congenital disorder of glycosylation Iy congenital myasthenic syndrome 22 severe congenital neutropenia 1 nonsyndromic congenital nail disorder autosomal dominant congenital deafness with onychodystrophy laryngomalacia TORCH syndrome rapidly involuting congenital hemangioma arthrogryposis multiplex congenita lethal congenital glycogen storage disease of heart congenital amegakaryocytic thrombocytopenia Leber congenital amaurosis 9 Leber congenital amaurosis 2 Leber congenital amaurosis 1 Leber congenital amaurosis 8 Leber congenital amaurosis 12 Leber congenital amaurosis 16 Leber congenital amaurosis 14 Leber congenital amaurosis 15 Leber congenital amaurosis 5 Leber congenital amaurosis 11 Leber congenital amaurosis 17 Leber congenital amaurosis 10 Leber congenital amaurosis 6 Leber congenital amaurosis 13 Leber congenital amaurosis 3 Leber congenital amaurosis 4 Leber congenital amaurosis 7 megaconial type congenital muscular dystrophy congenital muscular dystrophy 1B congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy due to LMNA mutation congenital myasthenic syndrome 8 congenital myasthenic syndrome 15 congenital myasthenic syndrome 7 congenital myasthenic syndrome 12 congenital myasthenic syndrome 20 congenital myasthenic syndrome 1B congenital myasthenic syndrome 1A congenital myasthenic syndrome 3C congenital myasthenic syndrome 3B congenital myasthenic syndrome 3A congenital myasthenic syndrome 5 congenital myasthenic syndrome 10 congenital myasthenic syndrome 14 congenital myasthenic syndrome 9 congenital myasthenic syndrome 6 congenital myasthenic syndrome 21 congenital myasthenic syndrome 19 congenital myasthenic syndrome 17 congenital myasthenic syndrome 11 congenital myasthenic syndrome 13 congenital myasthenic syndrome 4B congenital myasthenic syndrome 4A congenital myasthenic syndrome 4C congenital myasthenic syndrome 2C congenital myasthenic syndrome 2A congenital myasthenic syndrome 16 congenital myasthenic syndrome 18 congenital hypotrichosis with juvenile macular dystrophy congenital stationary night blindness 1G congenital stationary night blindness autosomal dominant 3 congenital stationary night blindness autosomal dominant 1 congenital stationary night blindness autosomal dominant 2 congenital stationary night blindness 1F congenital stationary night blindness 1B congenital stationary night blindness 1H congenital stationary night blindness 1C congenital stationary night blindness 1D congenital stationary night blindness 1E congenital stationary night blindness 1A congenital stationary night blindness 2A congenital bile acid synthesis defect 5 congenital bile acid synthesis defect 6 congenital bile acid synthesis defect 4 congenital bile acid synthesis defect 2 congenital bile acid synthesis defect 3 congenital bile acid synthesis defect 1 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital mirror movement disorder X-linked congenital myopathy with fiber-type disproportion congenital muscular dystrophy-dystroglycanopathy type A congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy-dystroglycanopathy type A9 congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A3 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A13 congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A2 congenital muscular dystrophy-dystroglycanopathy type A5 congenital muscular dystrophy-dystroglycanopathy type A6 palmoplantar keratoderma and congenital alopecia 1 palmoplantar keratoderma and congenital alopecia 2 congenital leptin deficiency epidermolysis bullosa with congenital localized absence of skin and deformity of nails large congenital melanocytic nevus congenital dyserythropoietic anemia type I congenital dyserythropoietic anemia type Ib congenital dyserythropoietic anemia type Ia congenital dyserythropoietic anemia type III congenital dyserythropoietic anemia type IV congenital dyserythropoietic anemia type II congenital vertical talus congenital heart defects, hamartomas of tongue, and polysyndactyly congenital contractural arachnodactyly congenital sucrase-isomaltase deficiency congenital lactase deficiency pancreatic hypoplasia-diabetes-congenital heart disease syndrome congenital nystagmus 1 congenital nystagmus 7 congenital nystagmus 2 congenital nystagmus 3 congenital nystagmus 6 congenital nystagmus 5 autosomal recessive congenital nystagmus linear skin defects with multiple congenital anomalies 1 congenital nongoitrous hypothyroidism 9 congenital nongoitrous hypothyroidism 7 congenital nongoitrous hypothyroidism 8 congenital disorder of glycosylation Icc X-linked congenital hemolytic anemia congenital bilateral absence of vas deferens X-linked congenital bilateral absence of vas deferens autosomal recessive congenital bilateral absence of vas deferens linear skin defects with multiple congenital anomalies 3 linear skin defects with multiple congenital anomalies 2 severe congenital encephalopathy due to MECP2 mutation congenital megabladder X-linked severe congenital neutropenia severe congenital neutropenia 7 autosomal dominant severe congenital neutropenia severe congenital neutropenia 2 severe congenital neutropenia 5 severe congenital neutropenia 3 severe congenital neutropenia 6 severe congenital neutropenia 8 severe congenital neutropenia 4 late congenital syphilis blepharophimosis congenital aphakia congenital toxoplasmosis congenital dyserythropoietic anemia congenital hypoplastic anemia congenital hypogammaglobulinemia Leber congenital amaurosis congenital heart disease myotonia congenita congenital afibrinogenemia congenital nonspherocytic hemolytic anemia congenital myasthenic syndrome congenital diaphragmatic hernia congenital structural myopathy congenital mesoblastic nephroma congenital disorder of glycosylation congenital hemolytic anemia congenital epulis cellular congenital mesoblastic nephroma classic congenital mesoblastic nephroma congenital granular cell tumor congenital fibrosarcoma non-congenital cyst of kidney congenital nystagmus congenital syphilis congenital heart block