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74765001: Lymphocyte count (procedure)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
124165010 Lymphocyte count en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
815300013 Lymphocyte count (procedure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634411000241111 numération lymphocytaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

17 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lymphocyte count Is a Blood cell count false Inferred relationship Some
Lymphocyte count Is a White blood cell test false Inferred relationship Some
Lymphocyte count Method Investigation - action false Inferred relationship Some
Lymphocyte count Has intent Diagnostic intent (qualifier value) false Inferred relationship Some
Lymphocyte count Has measured component (attribute) Lymphocyte false Inferred relationship Some
Lymphocyte count Component Hematology observable false Inferred relationship Some
Lymphocyte count Has specimen White blood cell specimen (specimen) false Inferred relationship Some
Lymphocyte count Component Lymphocyte true Inferred relationship Some 1
Lymphocyte count Method Evaluation - action false Inferred relationship Some
Lymphocyte count Method Measurement - action false Inferred relationship Some 2
Lymphocyte count Is a White blood cell count true Inferred relationship Some
Lymphocyte count Method Measurement - action true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Prolymphocyte count, blood Is a True Lymphocyte count Inferred relationship Some
Lymphocyte percent differential count Is a True Lymphocyte count Inferred relationship Some
B lymphocyte count Is a True Lymphocyte count Inferred relationship Some
T lymphocyte count Is a True Lymphocyte count Inferred relationship Some
Reactive lymphocyte count Is a True Lymphocyte count Inferred relationship Some
Lymphocyte count NOS Is a False Lymphocyte count Inferred relationship Some
Total lymphocyte count (IMM) Is a False Lymphocyte count Inferred relationship Some
Total T lymphocyte count (procedure) Is a False Lymphocyte count Inferred relationship Some
Natural killer cell level (procedure) Is a True Lymphocyte count Inferred relationship Some
Lymphocyte subset measurement (procedure) Is a True Lymphocyte count Inferred relationship Some
Lymphocyte count within reference range Interprets False Lymphocyte count Inferred relationship Some 1
Lymphocyte count outside reference range (finding) Interprets False Lymphocyte count Inferred relationship Some 1
Blood lymphocyte number above reference range (finding) Interprets False Lymphocyte count Inferred relationship Some 1
Lymphocyte count by cell surface antigen phenotype Is a True Lymphocyte count Inferred relationship Some
Lymphocyte count outside reference range (finding) Interprets True Lymphocyte count Inferred relationship Some 1
Blood lymphocyte number above reference range (finding) Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocyte count within reference range Interprets True Lymphocyte count Inferred relationship Some 1
Total lymphocyte count (procedure) Is a True Lymphocyte count Inferred relationship Some
Acquired lymphocytopenia (disorder) Interprets True Lymphocyte count Inferred relationship Some 2
Acquired lymphocytosis (disorder) Interprets True Lymphocyte count Inferred relationship Some 2
Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare, generally benign, lymphoproliferative hematological disease characterized by chronic, stable, persistent, polyclonal lymphocytosis of memory B-cell origin, the presence of binucleated lymphocytes in the peripheral blood, and a polyclonal increase in serum immunoglobulin M (IgM). Patients are most frequently asymptomatic or may present with mild splenomegaly. Interprets True Lymphocyte count Inferred relationship Some 1
Persistent lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocytic leukemoid reaction Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
T-cell lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocytosis - absolute (disorder) Interprets True Lymphocyte count Inferred relationship Some 1
Infectious lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
Monoclonal B-cell lymphocytosis (disorder) Interprets False Lymphocyte count Inferred relationship Some 1
Acute infectious lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocytopenia due to COVID-19 Interprets True Lymphocyte count Inferred relationship Some 1
Lymphopenia due to infection Interprets True Lymphocyte count Inferred relationship Some 1
Neonatal lymphocytopenia Interprets True Lymphocyte count Inferred relationship Some 3
Episodic lymphocytopenia Interprets True Lymphocyte count Inferred relationship Some 2
Lymphocytopenia Interprets True Lymphocyte count Inferred relationship Some 2
Panleukopenia (disorder) Interprets True Lymphocyte count Inferred relationship Some 3
Lymphocyte count below reference range Interprets True Lymphocyte count Inferred relationship Some 1
Relative lymphocytosis Interprets True Lymphocyte count Inferred relationship Some 1
Lymphocytes and monocytes, count, blood Is a True Lymphocyte count Inferred relationship Some
Percentage CD10 count (procedure) Is a True Lymphocyte count Inferred relationship Some
Plasma cell count Is a True Lymphocyte count Inferred relationship Some
A rare genetic immune disease characterized by early onset of recurrent bacterial, viral, and fungal infections, chronic inflammatory bowel disease, gastritis, and inflammatory polyarthritis. Patients present with diarrhea, vomiting, hepatosplenomegaly, mouth ulcers, perianal abscesses, chronic lung disease with bronchiectasis, and failure to thrive. Occurrence of a skin rash associated with lymphocytic vasculitis has also been reported. Immunologic abnormalities include variable T-cell lymphopenia, decreased natural killer cells, and decreased B-cells with variable hypogammaglobulinemia. Interprets True Lymphocyte count Inferred relationship Some 3
A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood. Interprets True Lymphocyte count Inferred relationship Some 3

This concept is not in any reference sets

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