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716697002: Hereditary persistence of alpha-fetoprotein (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3307234019 Hereditary persistence of alpha-fetoprotein (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3307235018 Hereditary persistence of alpha-fetoprotein en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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