Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4636398011 | Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4636399015 | Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Microcephaly | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Cortical blindness | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Chronic brain syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 3 | |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Finding site | Structure of Brodmann areas 17 (striate cortex), 18 (parastriate cortex) and 19 (peristriate cortex) of the occipital lobe | true | Inferred relationship | Existential restriction modifier | 4 | |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Interprets | Head circumference | true | Inferred relationship | Existential restriction modifier | 2 | |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Occurrence | Infancy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Finding site | Head structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR