Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4673264017 | MINDS syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4673265016 | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4673266015 | Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4673267012 | Smith Kingsmore syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4673268019 | MINDS (macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399612016 | A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability, characterized by macrocephaly, intellectual disability, seizures, dysmorphic facial features (including tall forehead, downslanting palpebral fissures, hypertelorism, depressed nasal bridge, and macrostomia), megalencephaly, and small thorax. Other reported features are umbilical hernia, muscular hypotonia, global developmental delay, autistic behavior, and café-au-lait spots, among others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399613014 | A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability, characterised by macrocephaly, intellectual disability, seizures, dysmorphic facial features (including tall forehead, downslanting palpebral fissures, hypertelorism, depressed nasal bridge, and macrostomia), megalencephaly, and small thorax. Other reported features are umbilical hernia, muscular hypotonia, global developmental delay, autistic behaviour, and café-au-lait spots, among others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Congenital macrocephaly (disorder) | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Seizure disorder | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Congenital anomaly of thorax | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Is a | Macroencephaly | true | Inferred relationship | Some | ||
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Finding site | Face structure | true | Inferred relationship | Some | 3 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Finding site | Thoracic structure | true | Inferred relationship | Some | 1 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Associated morphology | Congenital smallness | false | Inferred relationship | Some | 1 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Finding site | Cerebrum | true | Inferred relationship | Some | 2 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Associated morphology | Enlargement (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Interprets | Head circumference | true | Inferred relationship | Some | 4 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Has interpretation | Above reference range | true | Inferred relationship | Some | 4 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 5 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 6 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 6 | |
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome | Associated morphology | Abnormal smallness (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
Description inactivation indicator reference set