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890229002: Autosomal dominant polycystic liver disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4011651011 Autosomal dominant polycystic liver disease en Synonym Active Entire term case insensitive SNOMED CT core module
4011652016 Autosomal dominant polycystic liver disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Autosomal dominant polycystic liver disease Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant polycystic liver disease Is a Cyst of liver true Inferred relationship Existential restriction modifier
Autosomal dominant polycystic liver disease Is a Congenital anomaly of liver true Inferred relationship Existential restriction modifier
Autosomal dominant polycystic liver disease Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant polycystic liver disease Associated morphology Polycystic change true Inferred relationship Existential restriction modifier 1
Autosomal dominant polycystic liver disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant polycystic liver disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant polycystic liver disease Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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