716697002: Hereditary persistence of alpha-fetoprotein (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level\Protein level - finding\Alpha-fetoprotein level - finding\Alpha-fetoprotein raised\Hereditary persistence of alpha-fetoprotein
• \Measurement finding outside reference range\Measurement finding above reference range\Alpha-fetoprotein raised\Hereditary persistence of alpha-fetoprotein
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary persistence of alpha-fetoprotein
• \Disease\Chronic disease\Hereditary persistence of alpha-fetoprotein

Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3307234019	Hereditary persistence of alpha-fetoprotein (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3307235018	Hereditary persistence of alpha-fetoprotein	en	Synonym	Active	Case insensitive	SNOMED CT core
3307236017	A benign genetic condition with characteristic of persistence of high alpha-fetoprotein (AFP) levels throughout life, with no associated clinical disability and thus no need for specific therapy.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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