Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5099042016 | Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5099043014 | Lichtenstein Knorr syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 5099046018 | SCAR19 - spinocerebellar ataxia, autosomal recessive 19 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 5099048017 | Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5099049013 | Progressive autosomal recessive ataxia, deafness syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Decreased hearing | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Sensorineural hearing loss | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Chronic brain syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 | |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Finding site | Structure of auditory system | true | Inferred relationship | Existential restriction modifier | 4 | |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Interprets | Hearing, function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome | Has interpretation | Decreased | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR