Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3702087010 | Prader-Willi-like syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3702088017 | Prader-Willi-like syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
6q16 microdeletion syndrome | Is a | True | Prader-Willi-like syndrome | Inferred relationship | Existential restriction modifier | |
SIM bHLH transcription factor 1-related Prader-Willi-like syndrome | Is a | True | Prader-Willi-like syndrome | Inferred relationship | Existential restriction modifier | |
MAGE family member L2-related Prader-Willi-like syndrome | Is a | True | Prader-Willi-like syndrome | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets