699447001: syndroom van gingivale fibromatose, hepatosplenomegalie en andere anomalieën (aandoening)

SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Zimmermann-Laband syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2984508011 Zimmermann-Laband syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

2984623011 Zimmermann-Laband syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

2984767018 Laband-Zimmermann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

6396191000146111 Zimmermann-Laband-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

7011051000146112 syndroom van gingivale fibromatose, hepatosplenomegalie en andere anomalieën nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

7011061000146110 syndroom van gingivale fibromatose, hepatosplenomegalie en andere anomalieën (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Zimmermann-Laband syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets