Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1008611000172116 | syndrome de Hamano-Tsukamoto | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3705199011 | Hamano Tsukamoto syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3705202018 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3705203011 | Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 770371000241119 | syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 926351000172111 | syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3705200014 | A rare bulbospinal muscular atrophy characterised by generalised neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3705201013 | A rare bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome | localisation d'une constatation (attribut) | Structure of visual system (body structure) | true | Inferred relationship | Some | 2 | |
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome | localisation d'une constatation (attribut) | système nerveux | true | Inferred relationship | Some | 1 | |
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome | est un(e) (attribut) | atrophie musculaire spinale (trouble) | true | Inferred relationship | Some | ||
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome | est un(e) (attribut) | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome | est un(e) (attribut) | Ophthalmoplegia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR