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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.
Given the lack of knowledge of human infectious diseases at this time (and well into the 19th century) this was not an unusual conclusion, [15] but what is surprising is that while tulip mosaic disease has a far more impressive and documented history than any other plant virus, the realization that it was a communicable plant disease, let alone ...
The term childhood disease refers to disease that is contracted or becomes symptomatic before the age of 18 or 21 years old. Many of these diseases can also be contracted by adults. Some childhood diseases include:
List of ICD-9 codes 740–759: congenital anomalies ... Rare disease This page was last edited on 28 September 2024, at 13:01 (UTC). Text is available under the ...
Educating yourself about rare diseases can help spread the word and empathy.
List of childhood diseases and disorders; List of endocrine diseases; List of eponymous diseases; List of eye diseases and disorders; List of intestinal diseases; List of infectious diseases; List of human disease case fatality rates; List of notifiable diseases - diseases that should be reported to public health services, e.g., hospitals ...
Any disease that impacts 200,000 people or less in the U.S. is classified as a rare disease. The rare disease community is a close-knit group of patients, parents and specialists determined to ...
A rare disease is technically defined (in the European Union) as a disease that is found in fewer than 5 people per every 10,000 people. ...