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41326006: Classical galactosemia, heterozygous type (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
68934012 Classical galactosemia, heterozygous type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492965019 Classical galactosaemia, heterozygous type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
778102012 Classical galactosemia, heterozygous type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
68934012 Classical galactosemia, heterozygous type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
68934012 Classical galactosemia, heterozygous type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492965019 Classical galactosaemia, heterozygous type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
492965019 Classical galactosaemia, heterozygous type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
778102012 Classical galactosemia, heterozygous type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
778102012 Classical galactosemia, heterozygous type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4524901000241111 galactosémie de forme classique, hétérozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4524901000241111 galactosémie de forme classique, hétérozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Classical galactosemia, heterozygous type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase false Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, heterozygous type Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, heterozygous type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, heterozygous type Causative agent (attribute) UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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