Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 93289013 | Fascioscapulohumeral muscular dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 93290016 | Landouzy-Dejerine muscular dystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 93291017 | Landouzy-Déjérine muscular dystrophy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 93292012 | Facioscapulohumeral muscular dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 93293019 | Limb-girdle muscular dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 497510015 | FSH - Facioscapulohumeral muscular dystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 497511016 | FMD - Facioscapulohumeral muscular dystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 497512011 | FSHD - Facioscapulohumeral muscular dystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 794570010 | Facioscapulohumeral muscular dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Facioscapulohumeral muscular dystrophy | Is a | Autosomal dominant muscular dystrophy not predominantly limb girdle | false | Inferred relationship | Existential restriction modifier | ||
| Facioscapulohumeral muscular dystrophy | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
| Facioscapulohumeral muscular dystrophy | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Facioscapulohumeral muscular dystrophy | Associated morphology | Congenital anomaly | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets