Status: current, Not 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 |
| 3770071010 | Familial isolated hyperparathyroidism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3770072015 | Familial isolated hyperparathyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3770073013 | FIHPT - familial isolated hyperparathyroidism | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 8753261000146116 | familiaire geïsoleerde hyperparathyroïdie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8753271000146110 | familiaire geïsoleerde hyperparathyreoïdie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8753281000146112 | familiaire geïsoleerde hyperparathyreoïdie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3770074019 | A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumours in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumours and/or systemic manifestations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3770075018 | A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumors in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumors and/or systemic manifestations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial isolated hyperparathyroidism (disorder) | Interprets | Hormone secretion | true | Inferred relationship | Some | 1 | |
| Familial isolated hyperparathyroidism (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial isolated hyperparathyroidism (disorder) | Is a | Familial hyperparathyroidism | true | Inferred relationship | Some | ||
| Familial isolated hyperparathyroidism (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 1 | |
| Familial isolated hyperparathyroidism (disorder) | Is a | Hereditary disorder by system | false | Inferred relationship | Some | ||
| Familial isolated hyperparathyroidism (disorder) | Finding site | Parathyroid structure | true | Inferred relationship | Some | 2 | |
| Familial isolated hyperparathyroidism (disorder) | Due to | Neoplasm of parathyroid gland | true | Inferred relationship | Some | 3 | |
| Familial isolated hyperparathyroidism (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR