Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5401118015 | A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401119011 | A severe form of lissencephaly with cerebellar hypoplasia characterised by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3303812014 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303813016 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303814010 | Lissencephaly with cerebellar hypoplasia type C | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
6336161000241111 | LCHc - lissencéphalie avec hypoplasie cérébelleuse de type C | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6336171000241115 | lissencéphalie avec hypoplasie cérébelleuse congénitale de type C | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3432551001000114 | Lissenzephalie mit zerebellärer Hypoplasie Typ C | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Is a | Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) | true | Inferred relationship | Some | ||
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Associated morphology | anomalie congénitale | false | Inferred relationship | Some | 2 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Finding site | Brain structure | false | Inferred relationship | Some | 2 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Associated morphology | Hypoplasia | false | Inferred relationship | Some | 3 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)