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41326006: Classical galactosemia, heterozygous type (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
492965019 Classical galactosaemia, heterozygous type en Synonym Active Case insensitive SNOMED CT core
68934012 Classical galactosemia, heterozygous type en Synonym Active Case insensitive SNOMED CT core
778102012 Classical galactosemia, heterozygous type (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Classical galactosaemia, heterozygous type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase false Inferred relationship Some
Classical galactosaemia, heterozygous type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Some
Classical galactosaemia, heterozygous type Causative agent UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Some 1
Classical galactosaemia, heterozygous type Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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