111584000: Reticular dysgenesis (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\...
• \Measurement finding outside reference range\Abnormal blood cell count\White blood cell count abnormal (finding)\Decreased blood leukocyte number (finding)\Granulocyte count below reference range (finding)\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Abnormal blood cell count\White blood cell count abnormal (finding)\Decreased blood leukocyte number (finding)\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Abnormal blood cell count\White blood cell count abnormal (finding)\Neutrophil count abnormal\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Abnormal blood cell count\cytopénie (constatation)\Decreased blood leukocyte number (finding)\Granulocyte count below reference range (finding)\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Abnormal blood cell count\cytopénie (constatation)\Decreased blood leukocyte number (finding)\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Measurement finding below reference range (finding)\cytopénie (constatation)\Decreased blood leukocyte number (finding)\Granulocyte count below reference range (finding)\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Measurement finding outside reference range\Measurement finding below reference range (finding)\cytopénie (constatation)\Decreased blood leukocyte number (finding)\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \White blood cell number - finding\White blood cell count abnormal (finding)\...
• \Decreased blood leukocyte number (finding)\Granulocyte count below reference range (finding)\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Decreased blood leukocyte number (finding)\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Neutrophil count abnormal\neutropénie\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...
• \troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \anomalie de la lignée blanche\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \anomalie de la lignée blanche\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\troubles d'immunodéficience\Primary immune deficiency disorder (disorder)\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\troubles d'immunodéficience\Primary immune deficiency disorder (disorder)\Phagocytic cell defect\Disorder of phagocytic cell number\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\troubles d'immunodéficience\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\troubles d'immunodéficience\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\anomalie de la lignée blanche\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\trouble de la fonction immunitaire\anomalie de la lignée blanche\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée blanche\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée blanche\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
• \Disease\affection d'un système corporel\Disorder of immune structure (disorder)\Reticular dysgenesis
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
• \Disease\Congenital disease\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis
• \Disease\Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis

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
178837018	Reticular dysgenesis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363882019	De Vaal disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
363883012	Immunoerythromyeloid hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363884018	Severe combined immunodeficiency, neutropaenia and thrombocytopaenia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363885017	SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
363886016	Congenital aleukia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363887013	Reticular dysgenesia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363888015	Generalised haematopoietic hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363889011	Generalized hematopoietic hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3786555016	SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3786556015	Severe combined immunodeficiency, neutropenia and thrombocytopenia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
496751000241113	dysgénésie réticulaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
632826011	Reticular dysgenesis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
916681000172119	dysgénésie réticulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
948131000172115	aleucocytose congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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