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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
5893441000172111 galactosémie de forme classique, homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5143351000172115 homozygote Duarte-variant van GALT-genmutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
5143361000172118 homozygoot Duarte-type van deficiëntie van galactose-1-fosfaaturidylyltransferase nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
5143371000172110 homozygoot Duarte-type van deficiëntie van galactose-1-fosfaaturidyltransferase nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
5143381000172113 homozygote Duarte-variant van klassieke galactosemie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


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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