764946008: Constitutional mismatch repair deficiency syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary cancer-predisposing syndrome\Constitutional mismatch repair deficiency syndrome
• \Hereditary disorder by system\Hereditary disorder of immune system\Constitutional mismatch repair deficiency syndrome
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Constitutional mismatch repair deficiency syndrome
• \Disorder of immune function\Hereditary disorder of immune system\Constitutional mismatch repair deficiency syndrome
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Immunodeficiency associated with chromosomal abnormality\Constitutional mismatch repair deficiency syndrome
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Constitutional mismatch repair deficiency syndrome
• \Disorder of body system\Disorder of immune structure\Constitutional mismatch repair deficiency syndrome
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Constitutional mismatch repair deficiency syndrome
• \Congenital disease\Congenital immunodeficiency disease\Constitutional mismatch repair deficiency syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3655711013	Constitutional mismatch repair deficiency syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3655712018	CMMR-D (constitutional mismatch repair deficiency) syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3655713011	Constitutional mismatch repair deficiency syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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