238091006: Lecithin cholesterol acyltransferase deficiency (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocyte membrane abnormality\Lecithin cholesterol acyltransferase deficiency
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocyte membrane abnormality\Lecithin cholesterol acyltransferase deficiency
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Erythrocyte membrane abnormality\Lecithin cholesterol acyltransferase deficiency
• \Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\trouble de déficit en lipoprotéines\Hypoalphalipoproteinaemia\Lecithin cholesterol acyltransferase deficiency

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
356906011	Lecithin cholesterol acyltransferase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626925017	Lecithin cholesterol acyltransferase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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