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403829002: Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (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
1773757014 Familial hypercholesterolaemia due to heterozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1775043017 Familial hypercholesterolemia due to heterozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2972405018 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2972595014 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035741011 Familial hypercholesterolaemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1771755013 Familial hypercholesterolemia due to heterozygous LDL receptor mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1773757014 Familial hypercholesterolaemia due to heterozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1775043017 Familial hypercholesterolemia due to heterozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2972405018 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2972405018 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2972595014 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2972595014 Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035741011 Familial hypercholesterolaemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035741011 Familial hypercholesterolaemia due to heterozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6157091000241114 hypercholestérolémie familiale due à une mutation hétérozygote du récepteur des LDL (low density lipoprotein) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6157101000241117 hypercholestérolémie familiale due à une mutation hétérozygote du récepteur des lipoprotéines de basse densité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6157091000241114 hypercholestérolémie familiale due à une mutation hétérozygote du récepteur des LDL (low density lipoprotein) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6157101000241117 hypercholestérolémie familiale due à une mutation hétérozygote du récepteur des lipoprotéines de basse densité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Has definitional manifestation Serum cholesterol above reference range false Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation Interprets Serum total cholesterol measurement (procedure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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