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 | 
| 4634518013 | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 4634519017 | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Second cranial nerve finding | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Developmental delay | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Hereditary optic atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Cerebral atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Epilepsy | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 3 | |
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 | |
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Associated morphology | Primary atrophy | true | Inferred relationship | Existential restriction modifier | 2 | |
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Associated morphology | Diffuse atrophy | true | Inferred relationship | Existential restriction modifier | 1 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets