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403830007: Familial hypercholesterolemia due to homozygous 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
1773758016 Familial hypercholesterolaemia due to homozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1775044011 Familial hypercholesterolemia due to homozygous LDL receptor mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2972477013 Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2972813013 Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035909011 Familial hypercholesterolaemia due to homozygous low density lipoprotein receptor mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hypercholesterolaemia due to homozygous LDL receptor mutation est un(e) (attribut) Familial hypercholesterolemia (disorder) true Inferred relationship Some
Familial hypercholesterolaemia due to homozygous LDL receptor mutation localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Familial hypercholesterolaemia due to homozygous LDL receptor mutation est défini par la manifestation de (attribut) taux de cholestérol sérique augmenté false Inferred relationship Some
Familial hypercholesterolaemia due to homozygous LDL receptor mutation a pour interprétation (attribut) au-dessus de l'étendue de référence true Inferred relationship Some 1
Familial hypercholesterolaemia due to homozygous LDL receptor mutation interprète (attribut) Serum total cholesterol measurement (procedure) 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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