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719257008: Lathosterolosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3315711015 Lathosterolosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3315712010 Lathosterolosis en Synonym Active Entire term case insensitive SNOMED CT core module
3315713017 Sterol C5 desaturase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lathosterolosis Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Lathosterolosis Is a Disorder of cholesterol synthesis true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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