350353007: De Vaal's syndrome (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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Blood leukocyte number below reference range\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \Neutrophil count outside reference range\Neutropenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \White blood cell disorder\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \White blood cell disorder\Disorder of neutrophils\Quantitative abnormality of granulocytes\Quantitative disorder of neutrophils\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Disorder of immune function\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Disorder of immune function\White blood cell disorder\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Disorder of immune function\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Disorder of cellular component of blood\White blood cell disorder\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Disorder of cellular component of blood\White blood cell disorder\Leukopenia\Neutropenic disorder\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Disorder of body system\Disorder of immune structure\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Reticular dysgenesis\De Vaal's syndrome
• \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\De Vaal's syndrome
• \Disease\Congenital disease\Congenital immunodeficiency disease\Congenital neutropenia\Reticular dysgenesis\De Vaal's syndrome
• \Disease\Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent peripheral T cell maturation\Reticular dysgenesis\De Vaal's syndrome

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
472154017	De Vaal's syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
472155016	Immunodeficiency with generalized hematopoietic hypoplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
472156015	Immunodeficiency with generalised haematopoietic hypoplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
726304012	De Vaal's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2839405012	De Vaal syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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