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763668009: Lichtenstein syndrome (disorder)

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
3643231015 Lichtenstein syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3643232010 Lichtenstein syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lichtenstein syndrome Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier
Lichtenstein syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Lichtenstein syndrome Is a Phagocytic cell dysfunction true Inferred relationship Existential restriction modifier
Lichtenstein syndrome Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier
Lichtenstein syndrome Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
Lichtenstein syndrome Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Lichtenstein syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Lichtenstein syndrome Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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