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111584000: Reticular dysgenesis (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\...

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

\Decreased blood leucocyte number\Granulocyte count below reference range\Neutrophil count below reference range\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Decreased blood leucocyte number\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Neutrophil count abnormal\Neutrophil count below reference range\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis

\Finding of blood, lymphatics and immune system\Blood disease\...

\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\Leucopenia\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\SCID 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\SCID 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\SCID 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\SCID 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\Leucopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Blood disease\White blood cell disorder\Hereditary white blood cell disorder\Reticular dysgenesis
\Disease\Blood disease\White blood cell disorder\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis
\Disease\Blood disease\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\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\SCID 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\SCID due to absent peripheral T cell maturation\Reticular dysgenesis

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

178837018 Reticular dysgenesis en Synonym Active Case insensitive SNOMED CT core

363882019 De Vaal disease en Synonym Active Case sensitive SNOMED CT core

363883012 Immunoerythromyeloid hypoplasia en Synonym Active Case insensitive SNOMED CT core

363884018 Severe combined immunodeficiency, neutropaenia and thrombocytopaenia en Synonym Active Case insensitive SNOMED CT core

363885017 SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia en Synonym Active Case sensitive SNOMED CT core

363886016 Congenital aleukia en Synonym Active Case insensitive SNOMED CT core

363887013 Reticular dysgenesia en Synonym Active Case insensitive SNOMED CT core

363888015 Generalised haematopoietic hypoplasia en Synonym Active Case insensitive SNOMED CT core

363889011 Generalized hematopoietic hypoplasia en Synonym Active Case insensitive SNOMED CT core

3786555016 SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia en Synonym Active Case sensitive SNOMED CT core

3786556015 Severe combined immunodeficiency, neutropenia and thrombocytopenia en Synonym Active Case insensitive SNOMED CT core

632826011 Reticular dysgenesis (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Reticular dysgenesis with congenital aleucocytosis	Is a	True	Reticular dysgenesis	Inferred relationship	Some
De Vaal's syndrome	Is a	True	Reticular dysgenesis	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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