Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701261015 | ZASP (Z-band alternatively spliced PDZ motif protein) related myofibrillar myopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701262010 | Late-onset distal myopathy Markesbery Griggs type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3701263017 | ZASP related myofibrillar myopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701264011 | Late-onset distal myopathy Markesbery Griggs type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3701265012 | A rare genetic non-dystrophic myofibrillar myopathy disorder with characteristics of late-adult onset of distal and/or proximal limb muscle weakness with initial involvement of posterior lower leg muscles, medial gastrocnemius and soleus. Patients present with ankle weakness followed by weakness of finger and wrist extensors and later of the proximal muscles. Ambulation is usually preserved. Late-onset associated cardiomyopathy and/or neuropathy has been reported in a minority of cases. Caused by heterozygous mutation in the ZASP gene on chromosome 10. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Late-onset distal myopathy Markesbery Griggs type (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Late-onset distal myopathy Markesbery Griggs type (disorder) | Is a | Myofibrillar myopathy | true | Inferred relationship | Some | ||
| Late-onset distal myopathy Markesbery Griggs type (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
| Late-onset distal myopathy Markesbery Griggs type (disorder) | Occurrence | Adulthood | true | Inferred relationship | Some | 1 | |
| Late-onset distal myopathy Markesbery Griggs type (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR