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716698007: 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
3873311000052110 medfödd brist på alfafetoprotein sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

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

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