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190997006: Severe combined immunodeficiency with low T- and B-cell numbers (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
293705018 Severe combined immunodeficiency with low T- and B-cell numbers en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
574645011 Severe combined immunodeficiency with low T- and B-cell numbers (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe combined immunodeficiency with low T- and B-cell numbers Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 3
Severe combined immunodeficiency with low T- and B-cell numbers est un(e) (attribut) Disorder of immune structure (disorder) true Inferred relationship Some
Severe combined immunodeficiency with low T- and B-cell numbers est défini par la manifestation de (attribut) Immune system finding false Inferred relationship Some
Severe combined immunodeficiency with low T- and B-cell numbers est un(e) (attribut) Severe combined immunodeficiency disease true Inferred relationship Some
Severe combined immunodeficiency with low T- and B-cell numbers gravité (attribut) grave false Inferred relationship Some
Severe combined immunodeficiency with low T- and B-cell numbers localisation d'une constatation (attribut) structure du système immunitaire true Inferred relationship Some 1
Severe combined immunodeficiency with low T- and B-cell numbers survenue (attribut) congénital true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder) est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder) est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder) est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Severe combined immunodeficiency with hypereosinophilia (disorder) est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Severe combined immunodeficiency due to CTPS1 deficiency est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some
Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency est un(e) (attribut) True Severe combined immunodeficiency with low T- and B-cell numbers Inferred relationship Some

This concept is not in any reference sets

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