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721838005: Familial hypertryptophanemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3326199017 Familial hypertryptophanemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3326200019 Familial hypertryptophanemia en Synonym Active Entire term case insensitive SNOMED CT core module
3326207016 Familial hypertryptophanaemia 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
Familial hypertryptophanemia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial hypertryptophanemia Is a Familial disease true Inferred relationship Existential restriction modifier
Familial hypertryptophanemia Is a Tryptophanemia 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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