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Details
Link-It Detail - Disease - Aggressive Systemic Mastocytosis
Debug Stats
  • ### Total Build Time: 19 ms 20.328 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 411 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=7 ms Completed: 7 ms rowSize= 14.675 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.662 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Aggressive Systemic Mastocytosis C1112486
Definition (1)
A form of systemic mastocytosis in which patients have impaired organ functions due to multifocal infiltrates of pathological MAST CELLS in bone marrow, liver, spleen, gastrointestinal tract, or skeletal system. The cytomorphology shows a low to high grade.
Relationships (31)

Relation Types:
diso_​to_​anat : 12
diso_​to_​diso : 16
diso_​to_​phen : 3


Relationships:
is_​abnormal_​cell_​of_​disease : 5
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 4
is_​normal_​cell_​origin_​of_​disease : 3
is_​normal_​tissue_​origin_​of_​disease : 2
is_​not_​finding_​of_​disease : 3
is_​primary_​anatomic_​site_​of_​disease : 1
may_​be_​finding_​of_​disease : 9
may_​be_​molecular_​abnormality_​of_​disease : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_associated_anatomic_site_ofimg Bone Marrow C0005953
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Bone Marrow Stem Cell C1511246
DISO_to_ANATis_abnormal_cell_of_diseaseimg Cancer Cell C0334227
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Haematopoietic tissue C0229619
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Mast Cells C0024880
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cell C0597032
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Hematopoietic and Lymphoid Cell C1513983
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Mast Cell C1514012
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Myeloid Cell C1514039
DISO_to_DISOis_finding_of_diseaseimg Aggressive Clinical Course C1332223
DISO_to_DISOpermuted_term_ofimg Aggressive Systemic Mastocytosis C1112486
DISO_to_DISOmay_be_finding_of_diseaseimg Big spleen syndrome C0020532
DISO_to_DISOmay_be_molecular_abnormality_of_diseaseimg C-KIT Somatic Point Mutation C1511354
DISO_to_DISOmay_be_molecular_abnormality_of_diseaseimg C-KIT Tyrosine Kinase Protein Overexpression C1511355
DISO_to_DISOmay_be_finding_of_diseaseimg Cytopenia C0010828
DISO_to_DISOmay_be_finding_of_diseaseimg Enlarged Liver C0019209
DISO_to_DISOmay_be_finding_of_diseaseimg Enlarged Spleen C0038002
DISO_to_DISOmay_be_finding_of_diseaseimg Fractures, Spontaneous C0016663
DISO_to_DISOmay_be_finding_of_diseaseimg HYPERTENSION PORTAL C0020541
DISO_to_DISOis_not_finding_of_diseaseimg Ineffective Hematopoiesis C1334171
DISO_to_DISOmay_be_finding_of_diseaseimg Lytic lesion C0221204
DISO_to_DISOmay_be_finding_of_diseaseimg Malabsorption Syndrome C0024523
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanPTGES9536prostaglandin E synthase
img NCI, Score=801, Pubmed Id: 16299051, UMLKSK CUI: C1112486
HumanNTRK34916neurotrophic tyrosine kinase, receptor, type 3
img NCI, Score=801, Pubmed Id: 16648236, UMLKSK CUI: C1112486
HumanF2RL22151coagulation factor II (thrombin) receptor-like 2
img NCI, Score=801, Pubmed Id: 10409227, UMLKSK CUI: C1112486
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1112486Aggressive Systemic Mastocytosis0self