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61451000: Classical galactosemia, homozygous Negro-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
102092012 Classical galactosemia, homozygous Negro-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499013017 Classical galactosaemia, homozygous Negro-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800515019 Classical galactosemia, homozygous Negro-type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
102092012 Classical galactosemia, homozygous Negro-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
499013017 Classical galactosaemia, homozygous Negro-type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800515019 Classical galactosemia, homozygous Negro-type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5848771000241118 galactosémie classique, homozygote des populations d'origine africaine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5848781000241116 galactosémie classique, homozygote de type S135L fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5848771000241118 galactosémie classique, homozygote des populations d'origine africaine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5848781000241116 galactosémie classique, homozygote de type S135L fr Synonym (core metadata concept) Active Entire term case sensitive (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, homozygous Negro-type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase false Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, homozygous Negro-type Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, homozygous Negro-type Is a Deficiency of UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Existential restriction modifier (core metadata concept)
Classical galactosemia, homozygous Negro-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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