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1366635006: Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5460915016 Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5460916015 Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5460917012 Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene Is a Isolated polycystic liver disease (disorder) true Inferred relationship Some
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene Finding site Liver structure true Inferred relationship Some 1
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene Associated morphology Polycystic change true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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