Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 292944010 | Premature ageing syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 292945011 | Adult premature ageing syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 292946012 | Progeria syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 292947015 | Adult premature aging syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 292948013 | Premature aging syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 292949017 | Progeria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 574189012 | Progeria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progeria | Is a | Inborn error of metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Progeria | Is a | Congenital anomaly of integument | false | Inferred relationship | Existential restriction modifier | ||
| Progeria | Is a | Hereditary disorder of the integument | false | Inferred relationship | Existential restriction modifier | ||
| Progeria | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Progeria | Finding site | Skin structure | false | Inferred relationship | Existential restriction modifier | ||
| Progeria | Is a | Disorder of skin | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hutchinson-Gilford syndrome | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Acrogeria | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Infantile restrictive dermopathy | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Neonatal pseudo-hydrocephalic progeroid syndrome | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Wrinkly skin syndrome | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Geroderma osteodysplastica | Is a | False | Progeria | Inferred relationship | Existential restriction modifier | |
| Werner syndrome | Is a | False | Progeria | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets