Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3723057016 | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3723058014 | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 771051000241116 | syndrome de microcéphalie-polymicrogyrie-agénésie du corps calleux (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 907611000172111 | syndrome de microcéphalie-polymicrogyrie-agénésie du corps calleux | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3723059018 | A rare genetic central nervous system malformation syndrome with characteristics of marked prenatal-onset microcephaly, severe motor delay with hypotonia, bilateral polymicrogyria, corpus callosum agenesis, ventricular dilation, small cerebellum and early lethality. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | morphologie associée (attribut) | Congenital smallness | true | Inferred relationship | Some | 1 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | microgyrie (trouble) | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | agénésie du corps calleux (trouble) | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | localisation d'une constatation (attribut) | Structure of gyrus of brain (body structure) | true | Inferred relationship | Some | 1 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 2 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | syndrome de malformations multisystémiques | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | localisation d'une constatation (attribut) | Entire corpus callosum | true | Inferred relationship | Some | 2 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | morphologie associée (attribut) | Agenesis (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 3 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | interprète (attribut) | Birth head circumference | true | Inferred relationship | Some | 3 | |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | est un(e) (attribut) | Congenital microcephaly (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR