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403828005: Familial lipoprotein lipase deficiency with type V phenotype (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771754012 Familial lipoprotein lipase deficiency with type V phenotype (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782835012 Familial lipoprotein lipase deficiency with type V phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Is a Familial hyperchylomicronemia true Inferred relationship Some
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Finding site Body system structure false Inferred relationship Some
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Has definitional manifestation Serum lipids above reference range (finding) false Inferred relationship Some
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Has definitional manifestation Lipid above reference range false Inferred relationship Some
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Has interpretation Above reference range true Inferred relationship Some 1
Familial lipoprotein lipase deficiency with type V phenotype (disorder) Interprets Lipids measurement true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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