"Fanconi Anemia" 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.
Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004)
| Descriptor ID |
D005199
|
| MeSH Number(s) |
C15.378.071.085.080.280 C15.378.190.196.080.280 C16.320.077.280 C18.452.284.280
|
| Concept/Terms |
Fanconi Anemia- Fanconi Anemia
- Anemias, Fanconi
- Fanconi Anemias
- Fanconi's Anemia
- Anemia, Fanconi's
- Fanconi Pancytopenia
- Fanconi Panmyelopathy
- Anemia, Fanconi
- Fanconi Hypoplastic Anemia
|
Below are MeSH descriptors whose meaning is more general than "Fanconi Anemia".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Aplastic [C15.378.071.085]
- Anemia, Hypoplastic, Congenital [C15.378.071.085.080]
- Fanconi Anemia [C15.378.071.085.080.280]
- Bone Marrow Diseases [C15.378.190]
- Anemia, Aplastic [C15.378.190.196]
- Anemia, Hypoplastic, Congenital [C15.378.190.196.080]
- Fanconi Anemia [C15.378.190.196.080.280]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hypoplastic, Congenital [C16.320.077]
- Fanconi Anemia [C16.320.077.280]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- DNA Repair-Deficiency Disorders [C18.452.284]
- Fanconi Anemia [C18.452.284.280]
Below are MeSH descriptors whose meaning is more specific than "Fanconi Anemia".
This graph shows the total number of publications written about "Fanconi Anemia" by people in this website by year, and whether "Fanconi Anemia" 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 | 1 | 0 | 1 |
| 1999 | 2 | 0 | 2 |
| 2000 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2014 | 2 | 0 | 2 |
| 2015 | 0 | 1 | 1 |
| 2016 | 4 | 3 | 7 |
| 2017 | 7 | 2 | 9 |
| 2018 | 2 | 0 | 2 |
| 2019 | 0 | 2 | 2 |
| 2023 | 1 | 0 | 1 |
| 2024 | 2 | 0 | 2 |
| 2025 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Fanconi Anemia" by people in Profiles.
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Nuclear receptors regulate alternative lengthening of telomeres through a novel noncanonical FANCD2 pathway. Sci Adv. 2019 10; 5(10):eaax6366.
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Elevations in serum alpha fetoprotein levels in patients with Fanconi anaemia. Br J Haematol. 2019 03; 184(6):1032-1035.
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Expanding the FANCO/RAD51C associated phenotype: Cleft lip and palate and lobar holoprosencephaly, two rare findings in Fanconi anemia. Eur J Med Genet. 2018 May; 61(5):257-261.
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Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders. Clin Cancer Res. 2017 Jun 01; 23(11):e23-e31.
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UHRF1 contributes to DNA damage repair as a lesion recognition factor and nuclease scaffold. Cell Rep. 2015 Mar 31; 10(12):1957-66.
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FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions. Mol Cell. 2013 Mar 07; 49(5):997-1009.
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A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network. Mol Cell. 2012 Jul 13; 47(1):61-75.
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Fanconi anemia (FA) binding protein FAAP20 stabilizes FA complementation group A (FANCA) and participates in interstrand cross-link repair. Proc Natl Acad Sci U S A. 2012 Mar 20; 109(12):4491-6.
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Electronic monitoring feedback to promote adherence in an adolescent with Fanconi Anemia. Health Psychol. 2011 Sep; 30(5):503-9.
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Double-strand breaks induce homologous recombinational repair of interstrand cross-links via cooperation of MSH2, ERCC1-XPF, REV3, and the Fanconi anemia pathway. DNA Repair (Amst). 2007 Nov; 6(11):1670-8.