Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5234042018 | Familial multinodular goiter syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5234043011 | Familial multinodular goiter syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5234044017 | FMNG - familial multinodular goitre | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5234045016 | Familial multinodular goiter | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5234046015 | Familial multinodular goitre | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5234047012 | FMNG - familial multinodular goiter | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5234048019 | Familial multinodular goitre syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5234049010 | A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5234050010 | A rare thyroid disease characterised by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumours. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial multinodular goiter syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial multinodular goiter syndrome (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial multinodular goiter syndrome (disorder) | Is a | Multinodular goitre | true | Inferred relationship | Some | ||
| Familial multinodular goiter syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Familial multinodular goiter syndrome (disorder) | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Some | ||
| Familial multinodular goiter syndrome (disorder) | Finding site | Entire thyroid gland | true | Inferred relationship | Some | 1 | |
| Familial multinodular goiter syndrome (disorder) | Associated morphology | Enlargement (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Familial multinodular goiter syndrome (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 2 | |
| Familial multinodular goiter syndrome (disorder) | Associated morphology | Multinodular hyperplasia | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR