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1187616008: Deficiency of galactose mutarotase (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4674367018 Galactosemia type 4 en Synonym Active Entire term case insensitive SNOMED CT core module
4674368011 Galactosaemia type 4 en Synonym Active Entire term case insensitive SNOMED CT core module
4674369015 GALM (galactose mutarotase) deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
4674373017 Deficiency of galactose mutarotase en Synonym Active Entire term case insensitive SNOMED CT core module
4674374011 Deficiency of galactose mutarotase (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
Deficiency of galactose mutarotase Is a Galactosemia true Inferred relationship Existential restriction modifier
Deficiency of galactose mutarotase Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Deficiency of galactose mutarotase Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deficiency of galactose mutarotase Is a Inborn error of metabolism 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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