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 |
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 | |
Ocular albinism with congenital sensorineural deafness | 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