Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3755636014 | Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3755637017 | Asparagine synthetase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3755638010 | Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Cerebral atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Microcephalus | false | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Global developmental delay | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Inborn error of amino acid metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Congenital anomaly of brain | false | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Associated morphology | Congenital smallness | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Finding site | Brain structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Associated morphology | Atrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Congenital microcephaly | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Finding site | Head structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 3 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Interprets | Birth head circumference | true | Inferred relationship | Existential restriction modifier | 3 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 4 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 4 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 5 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 5 | |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR