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The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.
Pages in category "Genetic diseases and disorders" The following 187 pages are in this category, out of 187 total. This list may not reflect recent changes. ...
Most genetic disorders are rare in themselves. [5] [8] Genetic disorders are present before birth, and some genetic disorders produce birth defects, but birth defects can also be developmental rather than hereditary. The opposite of a hereditary disease is an acquired disease.
Legg–Calvé–Perthes disease; Legius syndrome; Leiner's disease; Lelis syndrome; Lemierre's syndrome; Lennox–Gastaut syndrome; Lenz microphthalmia syndrome; Lenz–Majewski syndrome; Leriche's syndrome; Leschke syndrome; Lesch–Nyhan syndrome; Lethal congenital contracture syndrome; Lethal white syndrome
List of congenital disorders. 1 language. ... List of ICD-9 codes 740–759: congenital anomalies; Rare disease This page was ...
List of notifiable diseases - diseases that should be reported to public health services, e.g., hospitals. Lists of plant diseases; List of pollution-related diseases; List of skin conditions; List of diseases by year of discovery; Disorders. List of communication disorders; List of genetic disorders; List of heart disorders; List of liver ...
Pages in category "Genetic syndromes" The following 164 pages are in this category, out of 164 total. ... Hirschsprung's disease-type D brachydactyly syndrome;
Category: Genetic disorders by system. 12 languages. ... Neurogenetic disorders (1 C, 27 P) This page was last edited on 26 October 2017, at 18:40 (UTC). ...