Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5159439011 | Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5159440013 | Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400416015 | A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by overgrowth and macrocephaly with megalencephaly apparent at birth, global developmental delay, intellectual disability, and dysmorphic facial features (including frontal bossing, long face, sparse eyebrows, hypertelorism, downslanting palpebral fissures, and prognathism). Patients may exhibit tall stature with dolichostenomelia, arachnodactyly, kyphoscoliosis, and joint laxity, as well as neurologic manifestations, such as hypotonia, gait ataxia, or seizures. Brain imaging may show increased white matter volume, thick corpus callosum, or small cerebellum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400417012 | A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by overgrowth and macrocephaly with megalencephaly apparent at birth, global developmental delay, intellectual disability, and dysmorphic facial features (including frontal bossing, long face, sparse eyebrows, hypertelorism, downslanting palpebral fissures, and prognathism). Patients may exhibit tall stature with dolichostenomelia, arachnodactyly, kyphoscoliosis, and joint laxity, as well as neurologic manifestations, such as hypotonia, gait ataxia, or seizures. Brain imaging may show increased white matter volume, thick corpus callosum, or small cerebellum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Congenital macrocephaly (disorder) | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Global developmental delay | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Multiple malformation syndrome with early overgrowth | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Is a | Macroencephaly | true | Inferred relationship | Some | ||
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Interprets | Head circumference | true | Inferred relationship | Some | 5 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Has interpretation | Above reference range | true | Inferred relationship | Some | 5 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Finding site | Cerebrum | true | Inferred relationship | Some | 1 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Associated morphology | Enlargement (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)