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238081000: Familial defective apolipoprotein B-100 (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356877019 FDB - Familial defective apolipoprotein B-100 en Synonym Active Case sensitive SNOMED CT core
356878012 Familial defective apolipoprotein B-100 en Synonym Active Initial character case insensitive SNOMED CT core
626914014 Familial defective apolipoprotein B-100 (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial defective apolipoprotein B-100 Has definitional manifestation Serum cholesterol raised false Inferred relationship Some
Familial defective apolipoprotein B-100 Occurrence Congenital false Inferred relationship Some
Familial defective apolipoprotein B-100 Finding site Body system structure false Inferred relationship Some
Familial defective apolipoprotein B-100 Is a Primary hypercholesterolaemia true Inferred relationship Some
Familial defective apolipoprotein B-100 Has interpretation Above reference range true Inferred relationship Some 1
Familial defective apolipoprotein B-100 Interprets Serum total cholesterol measurement true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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