Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma

Preferred Label : Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma;

NCIt synonyms : MALT Lymphoma of the Small Bowel; Small Intestine MALT Lymphoma; Small Bowel MALT Lymphoma; Small Intestine Mucosa-Associated Lymphoid Tissue Lymphoma; MALToma of Small Bowel; Small Bowel MALToma; Mucosa-Associated Lymphoid Tissue Lymphoma of Small Intestine; MALToma of the Small Bowel; Mucosa-Associated Lymphoid Tissue Lymphoma of Small Bowel; Small Intestine MALToma; Mucosa-Associated Lymphoid Tissue Lymphoma of the Small Intestine; MALT Lymphoma of Small Bowel; MALToma of Small Intestine; MALToma of the Small Intestine; Mucosa-Associated Lymphoid Tissue Lymphoma of the Small Bowel; Small Bowel Mucosa-Associated Lymphoid Tissue Lymphoma; MALT Lymphoma of the Small Intestine; MALT Lymphoma of Small Intestine;

NCIt definition : A mucosa-associated lymphoid tissue lymphoma (MALT) that arises from the small intestine. The morphologic characteristics are similar to those seen in gastric MALT lymphomas, with the exception of the lymphoepithelial lesions that are less prominent in the small intestine.;

Neoplastic status : Malignant;

Details

Origin ID

C5635;

UMLS CUI

C1336004;

Automatic exact mappings (from CISMeF team)
- Osteogenesis imperfecta [ORDO Disease]
Disease excludes abnormal cell
- Neoplastic T-Lymphocyte and Neoplastic Natural Killer Cell [NCIt concept]
- Reed-Sternberg Cell [NCIt concept]
Disease excludes normal cell origin
- Myeloid Cell [NCIt concept]
- Plasma Cell [NCIt concept]
- Precursor B-Lymphoblast [NCIt concept]
Disease may have findings
- Lymphoepithelial Lesion [NCIt concept]
Excludes anatomical site(s)
- Lymph Node [NCIt concept]
- Skin [NCIt concept]
False automatic mappings
- osteogenesis imperfecta [MeSH Descriptor]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
- Intestine [NCIt concept]
- Small Intestine [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Aggressive Clinical Course [NCIt concept]
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Abnormal Lymphocyte [NCIt concept]
- Centrocyte-Like Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic B-Lymphocyte [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
- Neoplastic Lymphocyte [NCIt concept]
disease_has_associated_disease
- Alpha Heavy Chain Disease [NCIt concept]
disease_has_finding
- Extranodal Disease [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_molecular_abnormality
- Clonal Immunoglobulin Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Heavy Chain Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Kappa Light Chain Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Lambda Light Chain Gene Rearrangement [NCIt concept]
disease_has_normal_cell_origin
- B-Lymphocyte [NCIt concept]
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Lymphocyte [NCIt concept]
- Marginal Zone B-Lymphocyte [NCIt concept]
- Mature B-Lymphocyte [NCIt concept]
- Postgerminal Center Marginal Zone B-Lymphocyte [NCIt concept]
disease_has_normal_tissue_origin
- Gut-Associated Lymphoid Tissue [NCIt concept]
- Hematopoietic and Lymphoid Tissue [NCIt concept]
- Lymphoid Tissue [NCIt concept]
- Marginal Zone [NCIt concept]
- Mucosa-Associated Lymphoid Tissue [NCIt concept]
- Small Intestinal Mucosa [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
- Lymphatic System [NCIt concept]
- Small Intestine [NCIt concept]
disease_mapped_to_gene
- BIRC3/MALT1 Fusion Gene [NCIt concept]
- MALT1 Gene [NCIt concept]
disease_may_have_abnormal_cell
- Neoplastic Monocytoid B-Lymphocyte [NCIt concept]
- Neoplastic Plasma Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Trisomy 18 [NCIt concept]
- Trisomy 3 [NCIt concept]
- t(1;14)(p22;q32) [NCIt concept]
pathogenesis_of_disease_involves_gene
- BIRC3/MALT1 Fusion Gene [NCIt concept]
- MALT1 Gene [NCIt concept]
- MALT1 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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