Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3737210015 | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3737212011 | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3747112019 | Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 4 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Associated morphology | Hyaline body | true | Inferred relationship | Existential restriction modifier | 1 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Disorder of macula of retina | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 4 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Microphthalmos | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Finding site | Entire eye | true | Inferred relationship | Existential restriction modifier | 2 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Associated morphology | Congenital smallness | true | Inferred relationship | Existential restriction modifier | 2 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Associated morphology | Separation | true | Inferred relationship | Existential restriction modifier | 3 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Finding site | Structure of fovea centralis | true | Inferred relationship | Existential restriction modifier | 3 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Retinal detachment | false | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Drusen of optic disc | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Finding site | Optic disc structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Inherited optic neuropathy | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Optic disc disorder | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Congenital retinoschisis | false | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome | Is a | Retinoschisis | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets