01
MRE11
MRE11 homolog, double strand break repair nuclease
MRE11 homolog, double strand break repair nuclease
Diseases
Nijmegen Breakage Syndrome-Like Disorder
nijmegen breakage syndrome-like disorder
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 3
Basic Information
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Core Information
- Disease Name
- Nijmegen Breakage Syndrome-Like Disorder
- Standard Disease Name
- nijmegen breakage syndrome-like disorder
- MeSH Tree
- No data
- ICD-10
- C91.4|C91.40
Identifiers
- DO ID
- No data
- MeSH ID
- D007943
- OMIM ID
- No data
- UMLS ID
- C0023443
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NCI-GLOSS_1602D:A rare type of leukemia in which abnormal B-lymphocytes (a type of white blood cell) are present in the bone marrow, spleen, and peripheral blood. When viewed under a microscope, these cells appear to be covered with tiny hair-like projections.|NCI2016_02D:A neoplasm of small B-lymphocytes with "hairy" projections in bone marrow, spleen, and peripheral blood. Most patients present with splenomegaly and pancytopenia. (WHO, 2001)|MSH2017_2016_08_12:A neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of "hairy" or "flagellated" cells in the blood and bone marrow.|CSP2006:neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of hairy or flagellated cells in the blood and bone marrow.
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