Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4673887017 | Autosomal dominant spastic paraplegia type 9B | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4673888010 | Autosomal dominant spastic paraplegia type 9B (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5399622010 | A rare predominantly pure hereditary spastic paraplegia characterized by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399623017 | A rare predominantly pure hereditary spastic paraplegia characterised by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4673887017 | Autosomal dominant spastic paraplegia type 9B | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4673888010 | Autosomal dominant spastic paraplegia type 9B (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4673889019 | A rare predominantly pure hereditary spastic paraplegia with characteristics of juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment and urinary symptoms. Cognition is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399622010 | A rare predominantly pure hereditary spastic paraplegia characterized by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399623017 | A rare predominantly pure hereditary spastic paraplegia characterised by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3447071001000114 | Spastische Paraplegie, autosomal-dominante, Typ 9B | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5808071000241111 | paraplégie spastique autosomique dominante de type 9B | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5808071000241111 | paraplégie spastique autosomique dominante de type 9B | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3447071001000114 | Spastische Paraplegie, autosomal-dominante, Typ 9B | 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)