About: Myelodysplastic Syndrome with Isolated del(5q)     Goto   Sponge   Distinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Myelodysplastic Syndrome with Isolated del(5q)
equivalentClass
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Myelodysplastic Syndrome with Isolated del(5q)
UMLS_CUI
  • C1292779
ALT_DEFINITION
  • A rare disorder caused by loss of part of the long arm (Q arm) of human chromosome 5. This syndrome affects myeloid (bone marrow) cells, causing treatment-resistant anemia, and myelodysplastic syndromes that may lead to acute myelogenous leukemia.NCI-GLOSS
ICD-O-3_Code
  • 9986/3
Neoplastic_Status
  • Undetermined
Legacy_Concept_Name
  • Myelodysplastic_Syndrome_Associated_with_Isolated_del_5q_Chromosome_Abnormality
FULL_SYN
  • 5Q minus syndromePTNCI-GLOSSCDR0000531047
  • 5q- SyndromeSYNCI
  • Myelodysplastic Syndrome with Isolated del(5q)SYNCITCGA
  • 5Q- syndromePTNCI-GLOSSCDR0000044810
  • Myelodysplastic Syndrome with Isolated del(5q)PTNCI
  • Myelodysplastic Syndrome Associated with Isolated del (5q) Chromosome AbnormalitySYNCI
  • Myelodysplastic Syndrome with 5q DeletionSYNCI
DEFINITION
  • A myelodysplastic syndrome characterized by a deletion between bands q31 and 33 on chromosome 5. The number of blasts in the bone marrow and blood is <5%. The bone marrow is usually hypercellular or normocellular with increased number of often hypolobated megakaryocytes. The peripheral blood shows macrocytic anemia. This syndrome occurs predominantly but not exclusively in middle age to older women. The prognosis is good and transformation to acute leukemia is rare. (WHO, 2001)NCI
code
  • C6867
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