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180485001: Kerasin thesaurismosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
279112018 Kerasin thesaurismosis en Synonym Active Entire term case insensitive SNOMED CT core module
563624014 Kerasin thesaurismosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Kerasin thesaurismosis Is a Hereditary disorder by system false Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Is a Metabolic disease false Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Finding site Body system structure false Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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