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