Preferred Label : Lymphocyte-Depleted Classic Hodgkin Lymphoma;
NCIt synonyms : Lymphocyte-Depleted Hodgkin's Disease; Lymphocyte Depleted Hodgkin Lymphoma; Hodgkin Lymphoma Lymphocyte Depleted; LDCHL; LDHL; Lymphocyte Depleted Hodgkin's Lymphoma; Hodgkin's Lymphoma Lymphocyte Depleted; Lymphocyte Depleted Classical Hodgkin's Lymphoma; Lymphocyte Depleted Hodgkin's Disease; Lymphocyte-Depleted Hodgkin's Lymphoma; Lymphocyte Depleted Hodgkin s Lymphoma; Hodgkin's Disease Lymphocyte Depletion; Lymphocyte Depleted Classical Hodgkin Lymphoma;
NCIt related terms : Hodgkin lymphoma, lymphocyte depletion, reticular; Lymphocyte-Depleted Classical Hodgkin Lymphoma; Classical Hodgkin lymphoma, lymphocyte depletion, diffuse fibrosis; Hodgkin lymphoma, lymphocyte depletion, diffuse fibrosis; Hodgkin Lymphoma, Lymphocyte Depletion, NOS; Lymphocyte depleted classical Hodgkin lymphoma, unspecified site;
NCIt definition : A diffuse subtype of classic Hodgkin lymphoma which is rich in Hodgkin and Reed-Sternberg
cells and/or depleted in non-neoplastic lymphocytes. (WHO, 2008);
Neoplastic status : Malignant;
ICD-O code : 9653/3; 9662/3;
Codes from synonyms : C81.30;
Origin ID : C9283;
UMLS CUI : C0152267;
- CISMeF manual mappings
- Currated CISMeF NLP mapping
- DO Cross reference
- Disease excludes normal cell origin
- Disease may have findings
- Has associated anatomic sites
- Semantic type(s)
- UMLS correspondences (same concept)
- concept_is_in_subset
- disease_excludes_finding
- disease_has_abnormal_cell
- disease_has_finding
- disease_has_normal_cell_origin
- disease_has_normal_tissue_origin
- disease_has_primary_anatomic_site
- disease_may_have_abnormal_cell
- disease_may_have_cytogenetic_abnormality
- disease_may_have_molecular_abnormality
- disease_may_have_normal_cell_origin