Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandLeukemia (D007938)
Parent Node:
expandMultiple Myeloma (D009101)
..Starting node
..expandLeukemia, Plasma Cell (D007952)

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..expandLeukemia, Plasma Cell (D007952)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6362
Name:Leukemia, Plasma Cell
Definition:A rare, aggressive variant of MULTIPLE MYELOMA characterized by the circulation of excessive PLASMA CELLS in the peripheral blood. It can be a primary manifestation of multiple myeloma or develop as a terminal complication during the disease.
Alternative IDs:
ParentIDs:MESH:D007938|MESH:D009101
TreeNumbers:C04.557.337.595 |C04.557.595.500.500 |C20.683.515.845.500
Synonyms:Leukemia, Plasmacytic |Leukemias, Plasma Cell |Leukemias, Plasmacytic |Plasma Cell Leukemia |Plasma Cell Leukemias |Plasmacytic Leukemia |Plasmacytic Leukemias
Slim Mappings:Cancer|Immune system disease
Reference: MedGen: D007952
MeSH: D007952
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants