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Items: 4

1.

Mast cell disease, systemic

A variant of mastocytosis characterized by multifocal, dense infiltrates of mast cells (15 or more mast cells in aggregates) detected in the bone marrow and/or other extracutaneous sites. (WHO, 2001) -- 2003 [from NCI]

MedGen UID:
67436
Concept ID:
C0221013
Disease or Syndrome
2.

Mastocytosis

The presence of an increased number of mast cells and CD34+ mast cell precursors in the body. [from HPO]

MedGen UID:
9902
Concept ID:
C0024899
Disease or Syndrome
3.

Mastocytosis

The presence of an increased number of mast cells and CD34+ mast cell precursors in the body. [from HPO]

MedGen UID:
451849
Concept ID:
CN117388
Finding
4.

Indolent systemic mastocytosis

An indolent mast cell neoplasm characterized by systemic infiltration of skin and internal organs by aggregates of neoplastic mast cells. There is no evidence of mast cell leukemia or clonal hematologic malignancy. Clinically, there is no evidence of palpable hepatomegaly and splenomegaly, malabsorption syndrome, or pathologic fractures. [from NCI]

MedGen UID:
82897
Concept ID:
C0272203
Disease or Syndrome
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