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10899004: Classical galactosemia, homozygous Duarte-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
18918012 Classical galactosemia, homozygous Duarte-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
332790010 Classical galactosaemia, homozygous Duarte-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
606980017 Classical galactosemia, homozygous Duarte-type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3800381000005110 klassisk galaktosæmi, homozygot Duarte-type da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) dansk modul


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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