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 |
3701926016 | Occult macular dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3701927013 | Occult macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3701928015 | OCMD - occult macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3701929011 | OMD - occult macular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3701931019 | A rare genetic retinal dystrophy disease with characteristics of bilateral progressive decline of visual acuity due to retinal dysfunction confined only to the macula, associated with normal fundus and fluorescein angiograms and severly attenuated focal macular and multifocal electroretinograms. There is evidence the disease is caused by heterozygous mutation in the RP1L1 gene on chromosome 8p23. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Occult macular dystrophy (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
Occult macular dystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Occult macular dystrophy (disorder) | Is a | Chronic disease | true | Inferred relationship | Some | ||
Occult macular dystrophy (disorder) | Finding site | Macula lutea structure | true | Inferred relationship | Some | 1 | |
Occult macular dystrophy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Occult macular dystrophy (disorder) | Is a | Hereditary macular dystrophy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets