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