"Anemia, Diamond-Blackfan" 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.
A rare congenital hypoplastic anemia that usually presents early in infancy. The disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia. (Curr Opin Hematol 2000 Mar;7(2):85-94)
| Descriptor ID |
D029503
|
| MeSH Number(s) |
C15.378.071.085.080.090 C15.378.071.750.500 C15.378.190.196.080.090 C16.320.077.090
|
| Concept/Terms |
Anemia, Diamond-Blackfan- Anemia, Diamond-Blackfan
- Anemia, Diamond Blackfan
- Anemia, Diamond-Blackfan Type
- Anemia, Diamond Blackfan Type
- Diamond-Blackfan Type Anemia
- Blackfan-Diamond Syndrome
- Blackfan Diamond Syndrome
- Diamond-Blackfan Anemia
- Diamond Blackfan Anemia
- Erythrogenesis Imperfecta
- Erythrogenesis Imperfectas
- Imperfecta, Erythrogenesis
- Imperfectas, Erythrogenesis
- Red Cell Aplasia, Pure, Hereditary
- Blackfan Diamond Anemia
- Anemia, Blackfan Diamond
- Diamond Anemia, Blackfan
- Blackfan-Diamond Disease
- Blackfan Diamond Disease
- Disease, Blackfan-Diamond
- Chronic Congenital Agenerative Anemia
- Congenital Erythroid Hypoplastic Anemia
- Congenital Hypoplastic Anemia of Blackfan and Diamond
- Congenital Pure Red Cell Anemia
- Congenital Pure Red Cell Aplasia
- Hypoplastic Congenital Anemia
- Anemia, Hypoplastic Congenital
- Anemias, Hypoplastic Congenital
- Congenital Anemia, Hypoplastic
- Congenital Anemias, Hypoplastic
- Hypoplastic Congenital Anemias
- Inherited Erythroblastopenia
- Erythroblastopenia, Inherited
- Erythroblastopenias, Inherited
- Inherited Erythroblastopenias
- Pure Hereditary Red Cell Aplasia
- Anemia, Congenital Hypoplastic, Of Blackfan And Diamond
|
Below are MeSH descriptors whose meaning is more general than "Anemia, Diamond-Blackfan".
- 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]
- Anemia, Diamond-Blackfan [C15.378.071.085.080.090]
- Red-Cell Aplasia, Pure [C15.378.071.750]
- Anemia, Diamond-Blackfan [C15.378.071.750.500]
- Bone Marrow Diseases [C15.378.190]
- Anemia, Aplastic [C15.378.190.196]
- Anemia, Hypoplastic, Congenital [C15.378.190.196.080]
- Anemia, Diamond-Blackfan [C15.378.190.196.080.090]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hypoplastic, Congenital [C16.320.077]
- Anemia, Diamond-Blackfan [C16.320.077.090]
Below are MeSH descriptors whose meaning is more specific than "Anemia, Diamond-Blackfan".
This graph shows the total number of publications written about "Anemia, Diamond-Blackfan" by people in this website by year, and whether "Anemia, Diamond-Blackfan" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Anemia, Diamond-Blackfan" by people in Profiles.
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Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder. Genomics. 2021 07; 113(4):1895-1905.
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Expansion of germline RPS20 mutation phenotype to include Diamond-Blackfan anemia. Hum Mutat. 2020 11; 41(11):1918-1930.
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Diamond-Blackfan anemia: death by heme toxicity? Eur J Haematol. 2016 Apr; 96(4):333-4.
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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia. J Med Genet. 2010 Nov; 47(11):777-81.
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Pneumocystis carinii pneumonia in patients with Diamond-Blackfan anemia receiving high-dose corticosteroids. J Pediatr Hematol Oncol. 2002 Jun-Jul; 24(5):410-2.