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403829002: Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1773757014 Familial hypercholesterolaemia due to heterozygous LDL receptor mutation en Synonym Active Initial character case insensitive SNOMED CT core
1775043017 Familial hypercholesterolemia due to heterozygous LDL receptor mutation en Synonym Active Initial character case insensitive SNOMED CT core
2972405018 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation en Synonym Active Case insensitive SNOMED CT core
2972595014 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3035741011 Familial hypercholesterolaemia due to heterozygous low density lipoprotein receptor mutation en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Is a Familial hypercholesterolaemia true Inferred relationship Some
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Finding site Body system structure false Inferred relationship Some
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Has definitional manifestation Serum cholesterol raised false Inferred relationship Some
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Has interpretation Above reference range true Inferred relationship Some 1
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation 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

Description inactivation indicator reference set

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