Status: current, Defined. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
102437010 | Congenital oculocutaneous hypopigmentation | en | Synonym | Active | Case insensitive | SNOMED CT core |
800734016 | Congenital oculocutaneous hypopigmentation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Ocular albinism with congenital sensorineural deafness | Is a | False | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
Waardenburg syndrome type 1 | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
Waardenburg syndrome type 2 | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
Vici syndrome | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
Osteoporosis and oculocutaneous hypopigmentation syndrome | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some | |
Oculocutaneous albinism | Is a | True | Congenital oculocutaneous hypopigmentation | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set