Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1770718019 | Heritable disorder of neutrophil function (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
1781886016 | Heritable disorder of neutrophil function | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Jung syndrome | Is a | True | Heritable disorder of neutrophil function | Inferred relationship | Existential restriction modifier | |
Siccardi syndrome | Is a | True | Heritable disorder of neutrophil function | Inferred relationship | Existential restriction modifier | |
Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome | Is a | True | Heritable disorder of neutrophil function | Inferred relationship | Existential restriction modifier | |
Neutrophil immunodeficiency syndrome | Is a | True | Heritable disorder of neutrophil function | Inferred relationship | Existential restriction modifier | |
Susceptibility to localized juvenile periodontitis | Is a | True | Heritable disorder of neutrophil function | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets