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890229002: Autosomal dominant polycystic liver disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. 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
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
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant polycystic liver disease Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant polycystic liver disease Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant polycystic liver disease Is a Liver cyst true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant polycystic liver disease Is a Congenital anomaly of liver true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant polycystic liver disease Finding site Liver structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant polycystic liver disease Associated morphology Polycystic change true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant polycystic liver disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant polycystic liver disease Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant polycystic liver disease Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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