Term Name: physical disorder
Synonyms: congenital disorder
Definition: A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.
Ontology: Human Disease [DOID:0080015]   ( DOID:0080015 )

Relationships
is a type of: disease
has subtype: agnathia-otocephaly complex arthrogryposis multiplex congenita autosomal dominant congenital deafness with onychodystrophy autosomal recessive congenital ichthyosis bladder exstrophy-epispadias-cloacal exstrophy complex blepharophimosis caudal regression syndrome cleft palate-lateral synechia syndrome Compton-North congenital myopathy congenital adrenal hyperplasia congenital adrenal insufficiency congenital afibrinogenemia congenital amegakaryocytic thrombocytopenia congenital aphakia congenital bilateral absence of vas deferens congenital bile acid synthesis defect congenital central hypoventilation syndrome congenital chylothorax congenital contractural arachnodactyly congenital diaphragmatic hernia congenital diarrhea congenital disorder of glycosylation congenital epulis congenital fibrosarcoma congenital fibrosis of the extraocular muscles congenital generalized lipodystrophy congenital granular cell tumor congenital heart block congenital heart defects, hamartomas of tongue, and polysyndactyly congenital heart disease congenital hemolytic anemia congenital hereditary endothelial dystrophy of cornea congenital hypogammaglobulinemia congenital hypoplastic anemia congenital hypothyroidism congenital hypotrichosis with juvenile macular dystrophy congenital intrinsic factor deficiency congenital lactase deficiency congenital leptin deficiency congenital megabladder congenital mesoblastic nephroma congenital mirror movement disorder congenital muscular dystrophy congenital myasthenic syndrome congenital myopathy 4A congenital nervous system abnormality congenital nystagmus congenital ptosis congenital secretory chloride diarrhea 1 congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congenital stationary night blindness congenital stromal corneal dystrophy congenital structural myopathy congenital sucrase-isomaltase deficiency congenital syphilis congenital toxoplasmosis congenital vertical talus cryptophthalmia developmental cardiac valvular defect epidermolysis bullosa with congenital localized absence of skin and deformity of nails gastroschisis Gollop-Wolfgang complex hypospadias imperforate anus Klippel-Feil syndrome large congenital melanocytic nevus laryngomalacia Leber congenital amaurosis lethal congenital contracture syndrome lethal congenital glycogen storage disease of heart linear skin defects with multiple congenital anomalies 1 linear skin defects with multiple congenital anomalies 2 linear skin defects with multiple congenital anomalies 3 Meckel's diverticulum multiple congenital anomalies-hypotonia-seizures syndrome myotonia congenita neonatal diabetes mellitus with congenital hypothyroidism neural tube defect non-congenital cyst of kidney nonsyndromic congenital nail disorder omphalocele orofacial cleft palmoplantar keratoderma and congenital alopecia 1 palmoplantar keratoderma and congenital alopecia 2 pancreatic hypoplasia-diabetes-congenital heart disease syndrome Poland syndrome polydactyly primary congenital glaucoma radioulnar synostosis rapidly involuting congenital hemangioma renal-hepatic-pancreatic dysplasia severe congenital encephalopathy due to MECP2 mutation severe congenital neutropenia Silver-Russell syndrome spondyloepiphyseal dysplasia with congenital joint dislocations T-cell immunodeficiency, congenital alopecia, and nail dystrophy TORCH syndrome visceral heterotaxy Zika virus congenital syndrome