402769003: Congenital/genetic syndrome with poikiloderma (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1770693017 Congenital/genetic syndrome with poikiloderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781863011 Congenital/genetic syndrome with poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1770693017 Congenital/genetic syndrome with poikiloderma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1770693017 Congenital/genetic syndrome with poikiloderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781863011 Congenital/genetic syndrome with poikiloderma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1781863011 Congenital/genetic syndrome with poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

85191000077116 poïkilodermie avec syndrome génétique ou congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

85191000077116 poïkilodermie avec syndrome génétique ou congénital 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
poïkilodermie avec syndrome génétique ou congénital	Is a	Secondary telangiectasia (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
poïkilodermie avec syndrome génétique ou congénital	Is a	Poikiloderma (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
poïkilodermie avec syndrome génétique ou congénital	Associated morphology	Telangiectasis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
poïkilodermie avec syndrome génétique ou congénital	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)
poïkilodermie avec syndrome génétique ou congénital	Finding site	Microscopic skin vascular structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
poïkilodermie avec syndrome génétique ou congénital	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
poïkilodermie avec syndrome génétique ou congénital	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
poïkilodermie avec syndrome génétique ou congénital	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
poïkilodermie avec syndrome génétique ou congénital	Associated morphology	Poikiloderma	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
poïkilodermie avec syndrome génétique ou congénital	Finding site	Microscopic skin vascular structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
poïkilodermie avec syndrome génétique ou congénital	Associated morphology	Telangiectasis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
poïkilodermie avec syndrome génétique ou congénital	Associated morphology	Poikiloderma	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
poïkilodermie avec syndrome génétique ou congénital	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary sclerosing poikiloderma of Weary (disorder)	Is a	False	poïkilodermie avec syndrome génétique ou congénital	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set