Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1767040019 | Infantile cataract (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1778580018 | Infantile cataract | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2446771000005116 | Infantil katarakt | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Infantile cataract (disorder) | Is a | Nonsenile cataract (disorder) | true | Inferred relationship | Some | ||
Infantile cataract (disorder) | Associated morphology | Opacity | true | Inferred relationship | Some | 1 | |
Infantile cataract (disorder) | Finding site | Lens clear | true | Inferred relationship | Some | 1 | |
Infantile cataract (disorder) | Associated morphology | Opacity | false | Inferred relationship | Some | 1 | |
Infantile cataract (disorder) | Finding site | Lens clear | false | Inferred relationship | Some | 1 | |
Infantile cataract (disorder) | Associated morphology | Katarakt | false | Inferred relationship | Some | 2 | |
Infantile cataract (disorder) | Finding site | Lens clear | false | Inferred relationship | Some | 2 | |
Infantile cataract (disorder) | Is a | Infantile and/or juvenile cataract | true | Inferred relationship | Some | ||
Infantile cataract (disorder) | Occurrence | Infancy | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome is characterized by congenital muscular dystrophy, infantile cataract and hypogonadism. It has been described in seven individuals from an isolated Norwegian village and in one unrelated individual. Transmission appears to be autosomal recessive. | Is a | True | Infantile cataract (disorder) | Inferred relationship | Some |
This concept is not in any reference sets