| familiaire geïsoleerde hyperparathyreoïdie (aandoening) | | familiaire geïsoleerde hyperparathyreoïdie | | familiaire geïsoleerde hyperparathyroïdie
| | Familial isolated hyperparathyroidism | | FIHPT - familial isolated hyperparathyroidism
| | A rare, hereditary, familial primary hyperparathyroidism disease characterized by 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. |
| | Id | 786037006 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E21.0 | | Term | Primaire hyperparathyroïdie |
|
| SNOMED CT to Orphanet simple map | 99879 |
| SNOMED CT to ICD-10 extended map | | Target | E21.0 | | Rule | TRUE | | Advice | ALWAYS E21.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
