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