Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
116327014 | Erythrokeratodermia variabilis | en | Synonym | Active | Case insensitive | SNOMED CT core |
1233217010 | Congenital poikiloderma | en | Synonym | Active | Case insensitive | SNOMED CT core |
1233218017 | Mendes da Costa syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
810054016 | Erythrokeratodermia variabilis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
MEDNIK syndrome | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
Keratoderma hereditarium mutilans with ichthyosis syndrome | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
Malignant atrophic papulosis | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set