716698007: congenitale deficiëntie 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 below reference range (finding)\Congenital deficiency of alpha-fetoprotein (disorder)

\Measurement finding outside reference range\Measurement finding below reference range (finding)\Alpha-fetoprotein below reference range (finding)\Congenital deficiency of alpha-fetoprotein (disorder)

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital deficiency of alpha-fetoprotein (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital deficiency 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

3307237014 Congenital deficiency of alpha-fetoprotein (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3307238016 Congenital deficiency of alpha-fetoprotein en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6202871000146110 congenitale deficiëntie van alfafoetoproteïne nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6202881000146112 congenitale deficiëntie van alfafoetoproteïne (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6202901000146110 aangeboren tekort aan AFP nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital deficiency of alpha-fetoprotein (disorder)	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
Congenital deficiency of alpha-fetoprotein (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Congenital deficiency of alpha-fetoprotein (disorder)	Is a	Alpha-fetoprotein below reference range (finding)	true	Inferred relationship	Some
Congenital deficiency of alpha-fetoprotein (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital deficiency of alpha-fetoprotein (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Congenital deficiency of alpha-fetoprotein (disorder)	Interprets	Alpha-1-Fetoprotein measurement (procedure)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets