Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
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 | Case insensitive | SNOMED CT core |
4634519017 | Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4634521010 | A rare severe early-onset neurodegenerative encephalopathy with main characteristic developmental delay/regression, epilepsy, cortical atrophy, secondary hypomyelination and thin corpus callosum. Additional features include secondary microcephaly, hypotonia, spasticity, optic atrophy and skeletal anomalies. This syndrome is caused by biallelic pathogenic variants in TBCD gene (17q25.3), encoding tubulin folding co-factor D (TBCD), one of five co-chaperones required for microtubule assembly dynamics. The pattern of inheritance is autosomal recessive. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Optic nerve finding | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Developmental delay | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Hereditary optic atrophy | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Cerebral atrophy | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Epilepsy | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 | |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 | |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 2 | |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome | Associated morphology | Diffuse atrophy | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set