Status: current. Date: 01-Jun 2025
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 |
| 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 | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene | Associated morphology | Polycystic change | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene | Finding site | Liver structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR