"Fatal Outcome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Death resulting from the presence of a disease in an individual, as shown by a single case report or a limited number of patients. This should be differentiated from DEATH, the physiological cessation of life and from MORTALITY, an epidemiological or statistical concept.
| Descriptor ID |
D017809
|
| MeSH Number(s) |
E05.318.308.985.550.325 N01.224.935.698.201 N06.850.505.400.975.550.325 N06.850.520.308.985.550.325
|
| Concept/Terms |
Fatal Outcome- Fatal Outcome
- Fatal Outcomes
- Outcome, Fatal
- Outcomes, Fatal
|
Below are MeSH descriptors whose meaning is more general than "Fatal Outcome".
Below are MeSH descriptors whose meaning is more specific than "Fatal Outcome".
This graph shows the total number of publications written about "Fatal Outcome" by people in this website by year, and whether "Fatal Outcome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 2 | 2 |
| 2004 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 2 | 2 |
| 2012 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 2 | 2 |
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click here.
Below are the most recent publications written about "Fatal Outcome" by people in Profiles.
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Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with caf?-au-lait spots. Fam Cancer. 2019 07; 18(3):353-358.
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Clearance of Treatment Refractory Adenoviremia via Adenovirus-specific Donor T-Cell Transfer During Aplasia After a?TCR-CD19-Depleted Stem Cell Transplantation. Clin Infect Dis. 2019 04 08; 68(8):1406-1409.
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Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy. J Med Genet. 2018 09; 55(9):637-640.
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Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN). Hum Mutat. 2017 11; 38(11):1477-1484.
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Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24. J Clin Immunol. 2016 10; 36(7):684-92.
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Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy. Brain. 2016 Feb; 139(Pt 2):338-45.
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Fatal outcome despite full lympho-hematopoietic reconstitution after allogeneic stem cell transplantation in atypical ataxia telangiectasia. J Clin Immunol. 2012 Jun; 32(3):438-40.
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Two adults with Rubinstein-Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers. Am J Med Genet A. 2009 Dec; 149A(12):2849-54.
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Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele. Neuromuscul Disord. 2009 Jul; 19(7):481-4.
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Prenatal ultrasound diagnosis, follow-up, and outcome of congenital varicella syndrome. Fetal Diagn Ther. 2006; 21(3):296-301.
MeSH information
