402783001: Congenital/hereditary cutis laxa (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1770707019 Congenital/hereditary cutis laxa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781877014 Congenital/hereditary cutis laxa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1770707019 Congenital/hereditary cutis laxa (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1770707019 Congenital/hereditary cutis laxa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781877014 Congenital/hereditary cutis laxa en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1781877014 Congenital/hereditary cutis laxa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital/hereditary cutis laxa	Is a	Cutis laxa	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital/hereditary cutis laxa	Finding site	Connective tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital/hereditary cutis laxa	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital/hereditary cutis laxa	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital/hereditary cutis laxa	Is a	Congenital connective tissue disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cutis laxa secondary to inherited disorder of connective tissue (disorder)	Is a	False	Congenital/hereditary cutis laxa	Inferred relationship	Existential restriction modifier (core metadata concept)
SCARF syndrome	Is a	False	Congenital/hereditary cutis laxa	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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

POSSIBLY EQUIVALENT TO association reference set