Primary Vitreoretinal Non-Hodgkin Lymphoma

Preferred Label : Primary Vitreoretinal Non-Hodgkin Lymphoma;

NCIt synonyms : PVRL; Primary Vitreoretinal Lymphoma;

NCIt definition : An uncommon and potentially fatal intraocular non-Hodgkin lymphoma that involves the uvea, retina, vitreous body, and optic nerve. It is a subset of primary central nervous system non-Hodgkin lymphoma. The majority of cases are diffuse large B-cell lymphomas.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL936835;

Details

Origin ID

C157065;

UMLS CUI

C4763388;

Disease excludes abnormal cell
- Reed-Sternberg Cell [NCIt concept]
Disease excludes normal cell origin
- Myeloid Cell [NCIt concept]
- Plasma Cell [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Eye [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Metastatic Lesion [NCIt concept]
disease_has_abnormal_cell
- Abnormal Lymphocyte [NCIt concept]
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
- Neoplastic Lymphocyte [NCIt concept]
disease_has_finding
- Intraocular Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Lymphocyte [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
- Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Eye [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
- Lymphatic System [NCIt concept]
- Vitreoretinal Area [NCIt concept]
disease_mapped_to_gene
- MYD88 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- MYD88 Gene Mutation [NCIt concept]
pathogenesis_of_disease_involves_gene
- MYD88 Gene [NCIt concept]
- MYD88 wt Allele [NCIt concept]

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