Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 116327014 | Erythrokeratodermia variabilis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 810054016 | Erythrokeratodermia variabilis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1233217010 | Congenital poikiloderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1233218017 | Mendes da Costa syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1886761000052119 | erythrokeratoderma variabilis (Mendes da Costa) | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Malignant atrophic papulosis | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
| Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some | |
| Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) | Is a | False | Erythrokeratodermia variabilis | Inferred relationship | Some |
This concept is not in any reference sets
FHIR