763668009: Lichtenstein syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of immune system\Lichtenstein syndrome
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Lichtenstein syndrome
• \Disorder of immune function (disorder)\Hereditary disorder of immune system\Lichtenstein syndrome
• \Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Phagocytic cell defect\Phagocytic cell dysfunction\Lichtenstein syndrome
• \Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Lichtenstein syndrome
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital immunodeficiency disease\Lichtenstein syndrome
• \Disorder of body system\Disorder of immune structure (disorder)\Lichtenstein syndrome
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Lichtenstein syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3643231015	Lichtenstein syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3643232010	Lichtenstein syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3643233017	Syndrome with characteristics of frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

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