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111584000: Reticular dysgenesis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis

\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\White blood cell disorder\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\White blood cell disorder\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Procedure related finding\Evaluation finding\Measurement finding\...

\White blood cell number - finding\White cell count abnormal\...

\Decreased blood leukocyte number\Granulocyte count below reference range (finding)\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Decreased blood leukocyte number\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Neutrophil count abnormal\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Phagocytic cell defect\Disorder of phagocytic cell number\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of body system\Disorder of immune structure\Reticular dysgenesis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of immune system\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Reticular dysgenesis	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Neutropenic disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Quantitative abnormality of granulocytes	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Finding site	Leucocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Reticular dysgenesis	Severity	Severe	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Reticular dysgenesis	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Associated morphology	White blood cell abnormality (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Disorder of immune structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Hereditary white blood cell disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Congenital neutropenia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has definitional manifestation	Neutropenia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	Neutropenic disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Reticular dysgenesis	Interprets	Neutrophil count	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Reticular dysgenesis	Pathological process (attribute)	Abnormal immune process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Reticular dysgenesis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Reticular dysgenesis	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Reticular dysgenesis with congenital aleucocytosis	Is a	True	Reticular dysgenesis	Inferred relationship	Existential restriction modifier (core metadata concept)
De Vaal's syndrome (disorder)	Is a	True	Reticular dysgenesis	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
632826011	Reticular dysgenesis (disorder)	en	Fully specified name	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
178837018	Reticular dysgenesis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character case insensitive (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	Only initial character 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	Only initial character case insensitive (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	Only initial character 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	Only initial character 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	Only initial character 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
632826011	Reticular dysgenesis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
632826011	Reticular dysgenesis (disorder)	en	Fully specified name	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
3388061001000119	Retikuläre Dysgenesie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
916681000172119	dysgénésie réticulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
948131000172115	aleucocytose congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
916681000172119	dysgénésie réticulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
948131000172115	aleucocytose congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3388061001000119	Retikuläre Dysgenesie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module