Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3755618014 | Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755619018 | SCAR20 - autosomal recessive spinocerebellar ataxia type 20 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755620012 | Autosomal recessive spinocerebellar ataxia type 20 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755621011 | Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
8502751000146113 | syndroom van verstandelijke beperking, grof aangezicht, macrocefalie en cerebellaire hypotrofie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8502761000146111 | syndroom van mentale retardatie, grof aangezicht, macrocefalie en cerebellaire hypotrofie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8502771000146117 | syndroom van verstandelijke beperking, grof aangezicht, macrocefalie en cerebellaire hypotrofie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8502781000146115 | syndroom van verstandelijke handicap, grof aangezicht, macrocefalie en cerebellaire hypotrofie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8603021000146117 | autosomaal recessieve spinocerebellaire ataxie type 20 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3755622016 | A rare genetic central nervous system malformation syndrome with characteristics of early-onset progressive severe cerebellar ataxia associated with progressive moderate to severe intellectual disability, global developmental delay, progressively coarsening facial features, relative macrocephaly and absence of seizures. Sensorineural hearing loss may be associated. Neuroimaging reveals cerebellar atrophy/hypoplasia. There is evidence the disease is caused by homozygous mutation in the SNX14 gene on chromosome 6q14. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Congenital cerebellar hypoplasia | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Hereditary ataxia (disorder) | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Global developmental delay | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Early onset cerebellar ataxia | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets