Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 406832013 | Tyrosinaemia-tyrosiluria hereditary syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 406833015 | Hereditary hypertyrosinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 406834014 | Hereditary hypertyrosinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 406835010 | Tyrosinemia-tyrosiluria hereditary syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 664301017 | Hereditary hypertyrosinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4554512018 | Hereditary tyrosinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4554513011 | Hereditary tyrosinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary hypertyrosinemia | Is a | Hypertyrosinemia | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary hypertyrosinemia | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary hypertyrosinemia | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary hypertyrosinemia | Is a | Hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary hypertyrosinemia | Is a | Hereditary metabolic disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Fumarylacetoacetase deficiency | Is a | False | Hereditary hypertyrosinemia | Inferred relationship | Existential restriction modifier | |
| Tyrosinemia type I | Is a | True | Hereditary hypertyrosinemia | Inferred relationship | Existential restriction modifier | |
| Fumarylacetoacetase deficiency, chronic type | Is a | True | Hereditary hypertyrosinemia | Inferred relationship | Existential restriction modifier | |
| Hypertyrosinemia, Richner-Hanhart type | Is a | True | Hereditary hypertyrosinemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR