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716697002: 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
5401366015 Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterized by 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
5401367012 Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterised by 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
3307234019 Hereditary persistence of alpha-fetoprotein (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
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
5401366015 Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterized by 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
5401367012 Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterised by 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
3411721001000112 Hereditäre Persistenz des Alpha-Fetoproteins de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
871231000172111 persistence héréditaire de l'alpha-foetoprotéine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
871231000172111 persistence héréditaire de l'alpha-foetoprotéine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411721001000112 Hereditäre Persistenz des Alpha-Fetoproteins de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

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 Existential restriction modifier (core metadata concept)
Hereditary persistence of alpha-fetoprotein (disorder) Is a Abnormal presence of alpha-fetoprotein false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of alpha-fetoprotein (disorder) Has interpretation Abnormal presence of false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary persistence of alpha-fetoprotein (disorder) Interprets Alpha-1-Fetoprotein measurement (procedure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary persistence of alpha-fetoprotein (disorder) Is a Chronic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of alpha-fetoprotein (disorder) Is a Alpha-fetoprotein above reference range (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of alpha-fetoprotein (disorder) Clinical course Chronic persistent true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary persistence of alpha-fetoprotein (disorder) Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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