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350353007: De Vaal's syndrome (disorder)

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

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

\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)

\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\White blood cell disorder\Disorder of neutrophils (disorder)\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)

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

\White blood cell number - finding\White blood cell count outside reference range\...

\Blood leukocyte number below reference range\Granulocyte count below reference range (finding)\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)

\Neutrophil count outside reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\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 (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\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\De Vaal's syndrome (disorder)
\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\De Vaal's syndrome (disorder)
\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\De Vaal's syndrome (disorder)
\Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\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\De Vaal's syndrome (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Disorder of neutrophils (disorder)\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Fetal and/or neonatal disorder\Congenital disease\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Fetal and/or neonatal disorder\Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Disorder of neutrophils (disorder)\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of body system\Disorder of immune structure (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)
\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 (disorder)\Reticular dysgenesis\De Vaal's syndrome (disorder)

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
De Vaal's syndrome (disorder)	Is a	Disorder of hematopoietic system	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Is a	Primary immune deficiency disorder	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Some	3
De Vaal's syndrome (disorder)	Is a	Reticular dysgenesis	true	Inferred relationship	Some
De Vaal's syndrome (disorder)	Finding site	Leukocyte	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
De Vaal's syndrome (disorder)	Severity	Severe	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Associated morphology	White blood cell abnormality	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Has definitional manifestation	Neutropenia	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
De Vaal's syndrome (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Some	1
De Vaal's syndrome (disorder)	Interprets	Neutrophil count	true	Inferred relationship	Some	1
De Vaal's syndrome (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
472154017	De Vaal's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
472155016	Immunodeficiency with generalized hematopoietic hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
472156015	Immunodeficiency with generalised haematopoietic hypoplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
726304012	De Vaal's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2839405012	De Vaal syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5220821000241117	syndrome de De Vaals	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module