Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770665016 | Skin damage resulting from congenital/hereditary neuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1781838011 | Skin damage resulting from congenital/hereditary neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Skin damage resulting from congenital/hereditary neuropathy | Is a | Dermatosis due to peripheral nerve disorder | false | Inferred relationship | Existential restriction modifier | ||
| Skin damage resulting from congenital/hereditary neuropathy | Finding site | Skin structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Skin damage resulting from congenital/hereditary neuropathy | Is a | Congenital disease | false | Inferred relationship | Existential restriction modifier | ||
| Skin damage resulting from congenital/hereditary neuropathy | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Skin damage resulting from congenital/hereditary neuropathy | Associated with | Peripheral nerve disease | false | Inferred relationship | Existential restriction modifier | ||
| Skin damage resulting from congenital/hereditary neuropathy | Due to | Peripheral nerve disease | false | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR