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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Classical galactosemia, homozygous Negro-type est un(e) (attribut) Deficiency of UTP-hexose-1-phosphate uridylyltransferase true Inferred relationship Some
Classical galactosemia, homozygous Negro-type Causative agent Uridine triphosphate-hexose-1-phosphate uridylyltransferase (substance) true Inferred relationship Some 1
Classical galactosemia, homozygous Negro-type est un(e) (attribut) Deficiency of UTP-hexose-1-phosphate uridylyltransferase false Inferred relationship Some
Classical galactosemia, homozygous Negro-type localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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