Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3009059013 | Lower motor neuron degeneration with Paget-like bone disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3009150010 | Pagetoid amyotrophic lateral sclerosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3009177018 | Muscular dystrophy limb-girdle with Paget disease of bone | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3009459019 | Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3009478019 | Pagetoid neuroskeletal syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3009492013 | Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3009710019 | IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Is a | Myopathy with cytoplasmic inclusions | true | Inferred relationship | Existential restriction modifier | ||
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 1 | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR