Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5403074016 | This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424676019 | Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3424677011 | Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3424678018 | PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424679014 | PHARC syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424680012 | Peripheral neuropathy Fiskerstrand type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
6476001000241115 | syndrome de polyneuropathie, surdité, ataxie, rétinite pigmentaire et cataracte | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6476011000241118 | neuropathie périphérique de type Fiskerstrand | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6476021000241113 | syndrome PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
602551000274116 | Periphere Neuropathie, Typ Fiskerstrand | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
602561000274118 | Polyneuropathie, Hörverlust, Ataxie, Retinitis pigmentosa und Katarakt | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3446231001000118 | Polyneuropathie - Hörverlust - Ataxie - Retinitis pigmentosa - Katarakt | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Polyneuropathy | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Autosomal recessive retinitis pigmentosa | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Disorder of lipid metabolism | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 2 | |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Finding site | Ear structure | false | Inferred relationship | Some | 1 | |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Associated morphology | Dystrophy | true | Inferred relationship | Some | 3 | |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Finding site | Retinal structure | true | Inferred relationship | Some | 3 | |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 1 | |
This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. | Interprets | Hearing | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)