FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

890229002: autosomaal dominante polycysteuze leverziekte (aandoening)


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
12249431000146114 autosomaal dominante polycysteuze leverziekte (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12249441000146118 autosomaal dominante polycysteuze leverziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12249451000146115 autosomaal dominante PCLD nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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 (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 (attribute) 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

GB English

US English

Back to Start