congenital
61Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency — Classification and external resources OMIM 202110 DiseasesDB 1841 …
62Congenital nephrotic syndrome — Classification and external resources ICD 10 N04 ICD 9 581.9 …
63Congenital generalized lipodystrophy — Classification and external resources eMedicine article/1113171 Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is a rare autosomal dominant skin condition, characterized by an extreme paucity of fat in the… …
64Congenital hypopituitarism — Classification and external resources ICD 10 Q89.2 ICD 9 759.2 …
65Congenital hearing loss — implies that the hearing loss is present at birth. It can include hereditary hearing loss or hearing loss due to other factors present either in utero (prenatal) or at the time of birth. Contents 1 Genetic factors 2 Hearing loss 2.1 Autosomal… …
66Congenital myasthenic syndrome — (CMS) is an inherited neuromuscular disorder caused by defects of several types at the neuromuscular junction. The effects of the disease are similar to Lambert Eaton syndrome and Myasthenia gravis, the difference being that CMS is not an… …
67Congenital dyserythropoietic anemia type I — (CDA I) is a disorder of blood cell production, particularly of the production of erythroblasts, which are the precursors of the red blood cells (RBCs).[1] Congenital dyserythropoietic anemia type I Classification and external resources ICD 10… …
68Congenital dyserythropoietic anemia type II — (CDA II), or HEMPAS is a rare genetic anaemia in humans characterized by hereditary erythroblastic multinuclearity with positive acidified serum lysis test.[1] Congenital dyserythropoietic anemia type II Classification and external resources ICD… …
69Congenital endothelial dystrophy type 2 — Classification and external resources A markedly opaque cornea due to stromal edema secondary to defective endothelial cells (Courtesy of Dr. Ahmed A. Hidajat) …
70Congenital fiber type disproportion — (CFTD) is an inherited form of myopathy with small type 1 muscle fibers that may occur in a number of neurological disorders.[1] It has a relatively good outcome and follows a stable course. [2] While the exact genetics is unclear there is an… …
