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61451000: Classical galactosemia, homozygous Negro-type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
102092012 Classical galactosemia, homozygous Negro-type en Synonym Active Only initial character case insensitive SNOMED CT core module
499013017 Classical galactosaemia, homozygous Negro-type en Synonym Active Only initial character case insensitive SNOMED CT core module
800515019 Classical galactosemia, homozygous Negro-type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core 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
Classical galactosemia, homozygous Negro-type Finding site Body system structure false Inferred relationship Existential restriction modifier
Classical galactosemia, homozygous Negro-type Is a Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase true Inferred relationship Existential restriction modifier
Classical galactosemia, homozygous Negro-type Causative agent Uridine triphosphate-hexose-1-phosphate uridylyltransferase true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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