763668009: Lichtenstein-syndroom (aandoening)

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

6245341000146111 Lichtenstein-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6245351000146114 syndroom van Lichtenstein nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10669681000146113 Lichtenstein-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lichtenstein syndrome	Is a	Congenital immunodeficiency disease	true	Inferred relationship	Some
Lichtenstein syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Lichtenstein syndrome	Is a	Phagocytic cell dysfunction	true	Inferred relationship	Some
Lichtenstein syndrome	Is a	Hereditary disorder of immune system	true	Inferred relationship	Some
Lichtenstein syndrome	Is a	Disorder of immune structure (disorder)	true	Inferred relationship	Some
Lichtenstein syndrome	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Some	1
Lichtenstein syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Lichtenstein syndrome	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2

Inbound Relationships

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Reference Sets

Description inactivation indicator reference set