Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321601013 | Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3321608019 | Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3321609010 | CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Early onset cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Inherited optic neuropathy | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Hereditary disorder of the visual system | false | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier | 3 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 4 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Finding site | Ear structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 4 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 4 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Congenital hearing disorder | false | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Disorder of ear | true | Inferred relationship | Existential restriction modifier | ||
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Interprets | Hearing, function | true | Inferred relationship | Existential restriction modifier | 5 | |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets