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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


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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