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414380008: Hawkinsinuria (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2530084012 Hawkinsinuria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2533521010 Hawkinsinuria en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hawkinsinuria Is a 4-Hydroxyphenylpyruvate dioxygenase deficiency true Inferred relationship Existential restriction modifier
Hawkinsinuria Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hawkinsinuria Is a Disorder of sulfur-bearing amino acid metabolism true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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