Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Olivopontocerebellar atrophy with slow eye movement | Is a | True | Olivopontocerebellar degeneration | Inferred relationship | Some | |
Olivopontocerebellar atrophy with blindness | Is a | True | Olivopontocerebellar degeneration | Inferred relationship | Some | |
Sporadic olivopontocerebellar atrophy (disorder) | Is a | True | Olivopontocerebellar degeneration | Inferred relationship | Some | |
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. | Is a | True | Olivopontocerebellar degeneration | Inferred relationship | Some |
This concept is not in any reference sets