890229002: Autosomal dominant polycystic liver disease (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4011651011 Autosomal dominant polycystic liver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4011652016 Autosomal dominant polycystic liver disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5807611000241111 affection polykystique du foie autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5807621000241116 maladie polykystique hépatique autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5807631000241119 polykystose hépatique autosomique dominante 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
polykystose hépatique autosomique dominante	Is a	Autosomal dominant hereditary disorder (disorder)	false	Inferred relationship	Some
polykystose hépatique autosomique dominante	Is a	Digestive system hereditary disorder	false	Inferred relationship	Some
polykystose hépatique autosomique dominante	Is a	Liver cyst	false	Inferred relationship	Some
polykystose hépatique autosomique dominante	Is a	Congenital anomaly of liver	false	Inferred relationship	Some
polykystose hépatique autosomique dominante	Finding site	Liver structure	false	Inferred relationship	Some	1
polykystose hépatique autosomique dominante	Associated morphology	Polycystic change	false	Inferred relationship	Some	1
polykystose hépatique autosomique dominante	Occurrence	Congenital	false	Inferred relationship	Some	1
polykystose hépatique autosomique dominante	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
polykystose hépatique autosomique dominante	Is a	Developmental hereditary disorder	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)