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 |
3447603012 | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447604018 | CAMOS syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3447605017 | CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3447606016 | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3447607013 | SCAR5 - spinocerebellar ataxia autosomal recessive 5 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403519011 | A disorder that is characterized by the association of a non-progressive congenital ataxia, severe intellectual deficit, optic atrophy and structural anomalies of the skin vessels. It has been described in five children from a large consanguineous Lebanese family. Short stature and microcephaly were also reported. Transmission is autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403520017 | A disorder that is characterised by the association of a non-progressive congenital ataxia, severe intellectual deficit, optic atrophy and structural anomalies of the skin vessels. It has been described in five children from a large consanguineous Lebanese family. Short stature and microcephaly were also reported. Transmission is autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Mental retardation | false | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Early onset cerebellar ataxia | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Inherited optic neuropathy | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Hereditary disorder of the visual system (disorder) | false | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Cutaneous vascular malformation (disorder) | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Congenital atrophy of optic nerve (disorder) | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 4 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Blood vessel structure of skin (body structure) | false | Inferred relationship | Some | 4 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 5 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Optic nerve structure | false | Inferred relationship | Some | 5 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Blood vessel structure of skin (body structure) | true | Inferred relationship | Some | 3 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Hereditary ataxia (disorder) | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Congenital anomaly of optic nerve | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Congenital degeneration of nervous system | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 4 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 5 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)