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716196007: Isolated polycystic liver disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5401259019 Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401260012 Isolated polycystic liver disease (PCLD) is a genetic disorder characterised by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3305052010 Isolated polycystic liver disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305053017 Isolated polycystic liver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5460914017 Autosomal dominant polycystic liver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
962361000172118 polykystose hépatique isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968531000172119 ADPCLD - autosomal dominant polycystic liver disease fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411121001000111 Lebererkrankheit, isolierte polyzystische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Is a Liver cyst true Inferred relationship Some
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Is a Digestive system hereditary disorder false Inferred relationship Some
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Associated morphology Polycystic change true Inferred relationship Some 1
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Finding site Liver structure true Inferred relationship Some 1
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Is a Genetic disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene Is a True Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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