Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 102437010 | Congenital oculocutaneous hypopigmentation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 800734016 | Congenital oculocutaneous hypopigmentation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Vici syndrome | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | |
| Osteoporosis and oculocutaneous hypopigmentation syndrome | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | |
| Oculocutaneous albinism | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | |
| Ocular albinism with congenital sensorineural deafness | Is a | False | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | |
| Waardenburg syndrome type 1 | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | |
| Waardenburg syndrome type 2 | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets