111584000: Reticular dysgenesis (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\...

\Measurement finding outside reference range\Blood cell count outside reference range\White blood cell count outside reference range\Blood leukocyte number below reference range\Granulocyte count below reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Blood cell count outside reference range\White blood cell count outside reference range\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Blood cell count outside reference range\White blood cell count outside reference range\Neutrophil count outside reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Blood leukocyte number below reference range\Granulocyte count below reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Blood leukocyte number below reference range\Granulocyte count below reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Finding of white blood cell number\White blood cell count outside reference range\...

\Blood leukocyte number below reference range\Granulocyte count below reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Neutrophil count outside reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\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\Reticular dysgenesis

\White blood cell disorder\Hereditary white blood cell 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\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\Reticular dysgenesis
\Disease\Disorder of immune function\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\Reticular dysgenesis
\Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\Reticular dysgenesis
\Disease\Disorder of immune function\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\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\Reticular dysgenesis
\Disease\Disorder of immune function\White blood cell disorder\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Disorder of immune function\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\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Hereditary white blood cell 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\Leukopenia\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\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\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\Reticular dysgenesis

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

Descriptions:

Id Description Lang Type Status Case? Module

178837018 Reticular dysgenesis en Synonym Active Entire term case insensitive SNOMED CT core module

363882019 De Vaal disease en Synonym Active Entire term case sensitive SNOMED CT core module

363883012 Immunoerythromyeloid hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module

363884018 Severe combined immunodeficiency, neutropaenia and thrombocytopaenia en Synonym Active Entire term case insensitive SNOMED CT core module

363885017 SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia en Synonym Active Entire term case sensitive SNOMED CT core module

363886016 Congenital aleukia en Synonym Active Entire term case insensitive SNOMED CT core module

363887013 Reticular dysgenesia en Synonym Active Entire term case insensitive SNOMED CT core module

363888015 Generalised haematopoietic hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module

363889011 Generalized hematopoietic hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module

632826011 Reticular dysgenesis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3786555016 SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia en Synonym Active Entire term case sensitive SNOMED CT core module

3786556015 Severe combined immunodeficiency, neutropenia and thrombocytopenia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Reticular dysgenesis with congenital aleukocytosis	Is a	True	Reticular dysgenesis	Inferred relationship	Existential restriction modifier
De Vaal's syndrome	Is a	True	Reticular dysgenesis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
178837018	Reticular dysgenesis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363882019	De Vaal disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
363883012	Immunoerythromyeloid hypoplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363884018	Severe combined immunodeficiency, neutropaenia and thrombocytopaenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363885017	SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
363886016	Congenital aleukia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363887013	Reticular dysgenesia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363888015	Generalised haematopoietic hypoplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
363889011	Generalized hematopoietic hypoplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
632826011	Reticular dysgenesis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3786555016	SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3786556015	Severe combined immunodeficiency, neutropenia and thrombocytopenia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module