loading...| Preferred Name |
Systemic Mastocytosis |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C9235 |
| ALT_DEFINITION |
A rare disease in which too many mast cells (a type of immune system cell) are found in the skin, bones, joints, lymph nodes, liver, spleen, and gastrointestinal tract. Mast cells give off chemicals such as histamine that can cause flushing (a hot, red face), itching, abdominal cramps, muscle pain, nausea, vomiting, diarrhea, low blood pressure, and shock. |
| code |
C9235 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 |
| Contributing_Source |
CTEP CTRP |
| DEFINITION |
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 |
| Display_Name |
Systemic Mastocytosis |
| FULL_SYN |
Systemic Tissue Mast Cell Disease Systemic mastocytosis, NOS |
| label |
Systemic Mastocytosis |
| Legacy_Concept_Name |
Systemic_Mastocytosis |
| Neoplastic_Status |
Malignant |
| Preferred_Name |
Systemic Mastocytosis |
| prefixIRI |
C9235 |
| prefLabel |
Systemic Mastocytosis |
| Semantic_Type |
Neoplastic Process |
| UMLS_CUI |
C0221013 |
| subClassOf |