Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2009. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2820529017 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2820530010 | Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2820531014 | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3702069012 | PEHO syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3702070013 | PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3702071012 | PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Disorder of brain | false | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Degenerative disease of the central nervous system | false | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Finding site | Brain structure | false | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Finding site | Brain structure | false | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Associated morphology | Lymphatic edema | true | Inferred relationship | Existential restriction modifier | 2 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Chronic brain syndrome | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Hereditary disorder of the visual system | false | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Degenerative brain disorder | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Second cranial nerve finding | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Hereditary lymphedema | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Finding site | Brain tissue structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Seizure disorder | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 3 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier | 4 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Inherited optic neuropathy | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 1 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier | ||
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Finding site | Limb structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets