Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3434553019 | Hereditary cerebral hemorrhage with amyloidosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3434554013 | Hereditary cerebral hemorrhage with amyloidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3434555014 | Hereditary cerebral haemorrhage with amyloidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3434556010 | HCHWA - hereditary cerebral hemorrhage with amyloidosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3434557018 | HCHWA - hereditary cerebral haemorrhage with amyloidosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary cerebral amyloid angiopathy, Icelandic type | Is a | True | Hereditary cerebral hemorrhage with amyloidosis | Inferred relationship | Existential restriction modifier | |
Hereditary cerebral amyloid angiopathy, Dutch type | Is a | True | Hereditary cerebral hemorrhage with amyloidosis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets