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890229002: Autosomal dominant polycystic liver disease (disorder)


Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4011651011 Autosomal dominant polycystic liver disease en Synonym Active Case insensitive SNOMED CT core
4011652016 Autosomal dominant polycystic liver disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core


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 Some
Autosomal dominant polycystic liver disease Is a Digestive system hereditary disorder true Inferred relationship Some
Autosomal dominant polycystic liver disease Is a Liver cyst true Inferred relationship Some
Autosomal dominant polycystic liver disease Is a Congenital anomaly of liver true Inferred relationship Some
Autosomal dominant polycystic liver disease Finding site Liver structure true Inferred relationship Some 1
Autosomal dominant polycystic liver disease Associated morphology Polycystic change true Inferred relationship Some 1
Autosomal dominant polycystic liver disease Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant polycystic liver disease Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant polycystic liver disease Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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