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 |
3303816012 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303817015 | Lissencephaly with cerebellar hypoplasia type D | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303818013 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5401120017 | A rare form of lissencephaly with cerebellar hypoplasia characterized by pronounced microcephaly (<= -3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401121018 | A rare form of lissencephaly with cerebellar hypoplasia characterised by pronounced microcephaly (<= -3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3303816012 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303817015 | Lissencephaly with cerebellar hypoplasia type D | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303818013 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303819017 | A form of lissencephaly with cerebellar hypoplasia with main features of pronounced microcephaly, intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401120017 | A rare form of lissencephaly with cerebellar hypoplasia characterized by pronounced microcephaly (<= -3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401121018 | A rare form of lissencephaly with cerebellar hypoplasia characterised by pronounced microcephaly (<= -3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3451481001000113 | Lissenzephalie mit zerebellärer Hypoplasie Typ D | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6396521000241119 | lissencéphalie avec hypoplasie cérébelleuse congénitale de type D | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6396531000241117 | LCHd - lissencéphalie avec hypoplasie cérébelleuse de type D | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6396521000241119 | lissencéphalie avec hypoplasie cérébelleuse congénitale de type D | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6396531000241117 | LCHd - lissencéphalie avec hypoplasie cérébelleuse de type D | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3451481001000113 | Lissenzephalie mit zerebellärer Hypoplasie Typ D | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
Description inactivation indicator reference set