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chromosome 5q deletion syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description 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)
Disease Ontology Description A chromosome deletion syndrome characterized by severe macrocytic anemia erythroid hypoplasia in the bone marrow, hypolobated micromegakaryocytes and that has material basis in somatic deletion of 1 allele of the RPS14, MIR145, MIR146A and/or DDX41 genes on chromosome 5q.
Mondo Term and Equivalent IDs
MONDO:0007925:  chromosome 5q deletion syndrome
COHD:136950: 
GARD:0008723: 
MESH:C535323: 
NCIT:C6867: 
Orphanet:86841: 
SCTID:277597005: 
UMLS:CN206233: