Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3310264019 | Pseudohypoparathyroidism type 1C (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3310265018 | Pseudohypoparathyroidism type 1C | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pseudohypoparathyroidism type 1C | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Pseudohypoparathyroidism type 1C | Is a | Pseudohypoparathyroidism | true | Inferred relationship | Existential restriction modifier | ||
Pseudohypoparathyroidism type 1C | Finding site | Parathyroid structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Pseudohypoparathyroidism type 1C | Interprets | Hormone secretion, function | true | Inferred relationship | Existential restriction modifier | 1 | |
Pseudohypoparathyroidism type 1C | Has interpretation | Decreased | true | Inferred relationship | Existential restriction modifier | 1 | |
Pseudohypoparathyroidism type 1C | Is a | Hereditary disorder by system | false | Inferred relationship | Existential restriction modifier | ||
Pseudohypoparathyroidism type 1C | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets