Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 102437010 | Congenital oculocutaneous hypopigmentation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 800734016 | Congenital oculocutaneous hypopigmentation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 1430331000052114 | medfödd okulokutan hypopigmentering | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Vici syndrome (disorder) | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
| Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
| Oculocutaneous albinism | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
| okulär albinism med kongenital sensorineural dövhet | Is a | False | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
| Waardenburg syndrome type 1 (disorder) | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
| Waardenburg syndrome type 2 (disorder) | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | 
This concept is not in any reference sets