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715923003: Lysosomal acid lipase deficiency (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304163017 LAL (Lysosomal acid lipase) deficiency en Synonym Active Case sensitive SNOMED CT core
3304164011 Lysosomal acid lipase deficiency en Synonym Active Case insensitive SNOMED CT core
3304165012 Lysosomal acid lipase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3305279019 LALD - Lysosomal acid lipase deficiency en Synonym Active Case sensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lysosomal acid lipase deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Lysosomal acid lipase deficiency Is a Inborn error of metabolism true Inferred relationship Some
Lysosomal acid lipase deficiency Is a Disorder of lipid storage and metabolism true Inferred relationship Some
Lysosomal acid lipase deficiency Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Cholesterol ester storage disease Is a True Lysosomal acid lipase deficiency Inferred relationship Some
Wolman's disease Is a True Lysosomal acid lipase deficiency Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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