Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3318852018 | Microphthalmia with brain atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3318853011 | Microphthalmia with brain atrophy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3318854017 | Syndromic microphthalmia type 10 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5308105019 | MOBA syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402304017 | A rare genetic neurodegenerative disorder characterized by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402305016 | A rare genetic neurodegenerative disorder characterised by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Microphthalmos | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Degenerative disorder | false | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Brain tissue structure | false | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Associated morphology | Congenital smallness | false | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Entire eye | false | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 3 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Brain tissue structure | false | Inferred relationship | Some | 3 | |
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Disorder of brain (disorder) | false | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Entire eye | false | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Associated morphology | Congenital smallness | false | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Degenerative brain disorder | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Entire eye proper | true | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Brain structure | true | Inferred relationship | Some | 2 | |
Microphthalmia with brain atrophy syndrome (disorder) | Associated morphology | Abnormal smallness (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Chronic disease of musculoskeletal system | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Seizure disorder | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Spasticity | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Severe intellectual disability (disorder) | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Disorder of skeletal muscle | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Microphthalmia with brain atrophy syndrome (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 6 | |
Microphthalmia with brain atrophy syndrome (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 7 | |
Microphthalmia with brain atrophy syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Microphthalmia with brain atrophy syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Microphthalmia with brain atrophy syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Microphthalmia with brain atrophy syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Microphthalmia with brain atrophy syndrome (disorder) | Interprets | Muscle tone | true | Inferred relationship | Some | 5 | |
Microphthalmia with brain atrophy syndrome (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 5 | |
Microphthalmia with brain atrophy syndrome (disorder) | Is a | Congenital blindness | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)