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 |
3302780011 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302781010 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302782015 | Olivopontocerebellar atrophy and deafness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400923011 | Olivopontocerebellar atrophy-deafness syndrome is characterized by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400924017 | Olivopontocerebellar atrophy-deafness syndrome is characterised by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302780011 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302780011 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302781010 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302781010 | Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302782015 | Olivopontocerebellar atrophy and deafness | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302782015 | Olivopontocerebellar atrophy and deafness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302783013 | Infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400923011 | Olivopontocerebellar atrophy-deafness syndrome is characterized by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400924017 | Olivopontocerebellar atrophy-deafness syndrome is characterised by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3395401001000117 | Olivopontozerebelläre Atrophie - Schwerhörigkeit | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3395401001000117 | Olivopontozerebelläre Atrophie - Schwerhörigkeit | 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)