761868000: Epigenetic disorder (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Epigenetic disorder

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3634089014 Epigenetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3634090017 Epigenetic disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3777278011 Changes in gene function that are mitotically and/or meiotically heritable and that do not entail a change in DNA sequence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3634089014 Epigenetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3634090017 Epigenetic disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3777278011 Changes in gene function that are mitotically and/or meiotically heritable and that do not entail a change in DNA sequence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

6095721000241118 affection épigénétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6095721000241118 affection épigénétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Epigenetic disorder	Is a	Hereditary disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Epigenetic disorder	Is a	Disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Imprinting error	Is a	True	Epigenetic disorder	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets