238078005: Familial hypercholesterolemia - homozygous (disorder)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Lipid level - finding\...

\Serum lipid levels - finding\Serum cholesterol level - finding\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Serum lipid levels - finding\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous

\Cholesterol level - finding\Serum cholesterol level - finding\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous

\Lipids abnormal\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Lipids abnormal\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Lipids abnormal\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous

\Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Measurement finding outside reference range\Lipids abnormal\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Measurement finding outside reference range\Lipids abnormal\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous
\Measurement finding outside reference range\Lipids abnormal\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous

\Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\troubles du stockage et du métabolisme des lipoprotéines\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia - homozygous

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3037192013 Familial homozygous hypercholesterolemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3037302012 Familial homozygous hypercholesterolaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356871018 Familial hypercholesterolemia - homozygous en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356872013 Familial hypercholesterolaemia - homozygous en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

549671000241115 hypercholestérolémie familiale homozygote (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

626911018 Familial hypercholesterolemia - homozygous (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

935951000172115 hypercholestérolémie familiale homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

975691000172119 hoFH - hypercholestérolémie familiale homozygote fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)