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 |
3302909015 | Mirror polydactyly, vertebral segmentation and limb defect syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302910013 | Mirror polydactyly, vertebral segmentation and limb defect syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400937019 | A rare disorder characterized by mirror polydactyly, vertebral hypersegmentation and severe congenital limb deficiencies. Duodenal atresia and absent thymus were also reported. So far, it has been described in four unrelated infants identified through a congenital malformation screening program carried out in Spain. The prevalence was estimated at around 1 in 330,000. The etiology is unknown but it was suggested that the syndrome is caused by defective expression of a developmental control gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400938012 | A rare disorder characterised by mirror polydactyly, vertebral hypersegmentation and severe congenital limb deficiencies. Duodenal atresia and absent thymus were also reported. So far, it has been described in four unrelated infants identified through a congenital malformation screening programme carried out in Spain. The prevalence was estimated at around 1 in 330,000. The aetiology is unknown but it was suggested that the syndrome is caused by defective expression of a developmental control gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302909015 | Mirror polydactyly, vertebral segmentation and limb defect syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302909015 | Mirror polydactyly, vertebral segmentation and limb defect syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302910013 | Mirror polydactyly, vertebral segmentation and limb defect syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302910013 | Mirror polydactyly, vertebral segmentation and limb defect syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302911012 | Rare syndrome with manifestations of mirror polydactyly, vertebral hypersegmentation and severe congenital limb deficiencies. Duodenal atresia and absent thymus also reported. So far, it has been described in four unrelated infants, it is suggested that the syndrome is caused by defective expression of a developmental control gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400937019 | A rare disorder characterized by mirror polydactyly, vertebral hypersegmentation and severe congenital limb deficiencies. Duodenal atresia and absent thymus were also reported. So far, it has been described in four unrelated infants identified through a congenital malformation screening program carried out in Spain. The prevalence was estimated at around 1 in 330,000. The etiology is unknown but it was suggested that the syndrome is caused by defective expression of a developmental control gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400938012 | A rare disorder characterised by mirror polydactyly, vertebral hypersegmentation and severe congenital limb deficiencies. Duodenal atresia and absent thymus were also reported. So far, it has been described in four unrelated infants identified through a congenital malformation screening programme carried out in Spain. The prevalence was estimated at around 1 in 330,000. The aetiology is unknown but it was suggested that the syndrome is caused by defective expression of a developmental control gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3381431001000111 | Polydaktylie, spiegelbildliche - vertebrale Segmentierungsdefekte - Extremitätenanomalien | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1015851000172111 | syndrome de polydactylie en miroir-segmentation vertébrale-anomalies des membres | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1015851000172111 | syndrome de polydactylie en miroir-segmentation vertébrale-anomalies des membres | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3381431001000111 | Polydaktylie, spiegelbildliche - vertebrale Segmentierungsdefekte - Extremitätenanomalien | 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)