716697002: hereditaire persistentie van alfafoetoproteïne (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Protein level - finding\Alpha-fetoprotein level - finding\Alpha-fetoprotein above reference range (finding)\Hereditary persistence of alpha-fetoprotein (disorder)

\Measurement finding outside reference range\Measurement finding above reference range\Alpha-fetoprotein above reference range (finding)\Hereditary persistence of alpha-fetoprotein (disorder)

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary persistence of alpha-fetoprotein (disorder)
\Disease\Chronic disease\Hereditary persistence of alpha-fetoprotein (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3307235018 Hereditary persistence of alpha-fetoprotein en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6361171000146119 hereditaire persistentie van alfafoetoproteïne nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6361181000146117 hereditaire persistentie van alfafoetoproteïne (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6361191000146115 erfelijke persistentie van AFP nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary persistence of alpha-fetoprotein (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary persistence of alpha-fetoprotein (disorder)	Is a	Abnormal presence of alpha-fetoprotein	false	Inferred relationship	Some
Hereditary persistence of alpha-fetoprotein (disorder)	Has interpretation	Abnormal presence of	false	Inferred relationship	Some	1
Hereditary persistence of alpha-fetoprotein (disorder)	Interprets	Alpha-1-Fetoprotein measurement (procedure)	true	Inferred relationship	Some	1
Hereditary persistence of alpha-fetoprotein (disorder)	Is a	Chronic disease	true	Inferred relationship	Some
Hereditary persistence of alpha-fetoprotein (disorder)	Is a	Alpha-fetoprotein above reference range (finding)	true	Inferred relationship	Some
Hereditary persistence of alpha-fetoprotein (disorder)	Clinical course	Chronic persistent	true	Inferred relationship	Some	2
Hereditary persistence of alpha-fetoprotein (disorder)	Has interpretation	Above reference range	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets