Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 378441011 | Erythrokeratoderma | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 645076019 | Erythrokeratoderma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypotrichosis and deafness syndrome | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Mutilating keratoderma | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Erythrokeratodermia cardiomyopathy syndrome | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Erythrokeratoderma en cocardes | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Congenital keratoderma | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Erythrokeratodermia variabilis | Is a | False | Erythrokeratoderma | Inferred relationship | Some | |
| Ichthyosiform erythroderma | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Erythrokeratoderma progressiva of Gottron | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| Spinocerebellar ataxia type 34 | Is a | True | Erythrokeratoderma | Inferred relationship | Some | |
| MEDNIK syndrome | Is a | False | Erythrokeratoderma | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set