Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
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Parent Node:
expandLeukemia (D007938)
Parent Node:
expandLeukemia, Myeloid, Acute (D015470)
Parent Node:
expandMastocytosis, Systemic (D034721)
..Starting node
..expandLeukemia, Mast-Cell (D007946)

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..expandLeukemia, Mast-Cell (D007946)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6347
Name:Leukemia, Mast-Cell
Definition:A form of systemic mastocytosis (MASTOCYTOSIS, SYSTEMIC) characterized by the presence of large numbers of tissue MAST CELLS in the peripheral blood without skin lesions. It is a high-grade LEUKEMIA disease with bone marrow smear of >20% MAST CELLS, multi-organ failure and a short survival.
Alternative IDs:
ParentIDs:MESH:D007938|MESH:D015470|MESH:D034721
TreeNumbers:C04.557.337.440 |C04.557.337.539.275.440 |C04.557.450.565.465.750.500
Synonyms:Leukemia, Mast Cell |Leukemias, Mast-Cell |Mast Cell Leukemia |Mast-Cell Leukemia |Mast-Cell Leukemias
Slim Mappings:Cancer
Reference: MedGen: D007946
MeSH: D007946
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants