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1237346001: Caroli syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5097825015 Caroli syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5097826019 Caroli syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Caroli syndrome Is a Cystic dilation of intrahepatic duct true Inferred relationship Existential restriction modifier
Caroli syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Caroli syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Caroli syndrome Is a Congenital hepatic fibrosis true Inferred relationship Existential restriction modifier
Caroli syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Caroli syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Caroli syndrome Finding site Liver structure true Inferred relationship Existential restriction modifier 1
Caroli syndrome Associated morphology Fibrosis true Inferred relationship Existential restriction modifier 1
Caroli syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Caroli syndrome Finding site Structure of wall of intrahepatic biliary tract true Inferred relationship Existential restriction modifier 2
Caroli syndrome Associated morphology Cystic dilatation true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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