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 |
3303822015 | Lissencephaly with cerebellar hypoplasia type F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303824019 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303825018 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5401122013 | A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401123015 | A severe form of lissencephaly with cerebellar hypoplasia, characterised by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3303822015 | Lissencephaly with cerebellar hypoplasia type F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303824019 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303825018 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303823013 | A severe form of lissencephaly with cerebellar hypoplasia with main features microcephaly of at least 3 standard deviations and a thick cortex associated with complete absence of the corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401122013 | A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401123015 | A severe form of lissencephaly with cerebellar hypoplasia, characterised by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3441711001000110 | Lissenzephalie mit zerebellärer Hypoplasie Typ F | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366481000241117 | lissencéphalie avec hypoplasie cérébelleuse congénitale de type F | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366491000241115 | LCHf - lissencéphalie avec hypoplasie cérébelleuse de type F | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366481000241117 | lissencéphalie avec hypoplasie cérébelleuse congénitale de type F | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366491000241115 | LCHf - lissencéphalie avec hypoplasie cérébelleuse de type F | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3441711001000110 | Lissenzephalie mit zerebellärer Hypoplasie Typ F | 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)