Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 31905016 | Niemann-Pick disease, type D | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 31906015 | Niemann-Pick disease, Nova Scotian | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 746553016 | Niemann-Pick disease, type D (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 1222212015 | Niemann-Pick disease type D | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3038211012 | Niemann pick disease type D | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Niemann-Pick disease, type D | Is a | Sphingomyelin/cholesterol lipidosis | true | Inferred relationship | Existential restriction modifier | ||
| Niemann-Pick disease, type D | Associated morphology | Niemann-Pick cell | false | Inferred relationship | Existential restriction modifier | ||
| Niemann-Pick disease, type D | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Niemann-Pick disease, type D | Associated morphology | Foam cell | false | Inferred relationship | Existential restriction modifier | ||
| Niemann-Pick disease, type D | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR