ORPHA:68415
Rare parathyroid disease and phosphocalcic metabolism anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare parathyroid disease and phosphocalcic metabolism anomaly | |
| fr | Maladie parathyroïdienne rare et anomalie du métabolisme phosphocalcique | |
| de | Nebenschilddrüse und Calcium/Phosphor-Stoffwechselkrankheit, seltene | |
| es | Enfermedades paratiroideas raras y trastornos del metabolismo fosfocálcico | |
| it | Malattia del metabolismo fosfocalcico | |
| nl | Zeldzame bijschildklierziekte en fosfocalcaire stofwisselingsstoornis | |
| pt | Doença da paratiroide e anomalia do metabolismo fosfo-cálcico rara | |
| pl | Rzadkie choroby przytarczyc i zaburzenia metabolizmu fosforanowo-wapniowego | |
| cs | Vzácná paratyreoidální nemoc a anomálie kalciofosfátového metabolismu | |
| uk | Рідкісне захворювання паращитовидної залози та аномалія фосфокальцієвого обміну | |
| zh | 罕见甲状旁腺疾病伴磷钙代谢异常 | |
| tr | Nadir paratiroid hastalığı ve fosfokalsik metabolizma anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19061 | E | validated | |
| UMLS | C5681339 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:97978Rare endocrine disease
rare endocrine diseases
Children (8):
- ORPHA:300547Autosomal recessive infantile hypercalcemia
- ORPHA:289098Disorders of vitamin D metabolism
- ORPHA:405Familial hypocalciuric hypercalcemia
- ORPHA:53715Familial tumoral calcinosis
- ORPHA:352540Oncogenic osteomalacia
- ORPHA:181408Rare hyperparathyroidism
- ORPHA:181405Rare hypoparathyroidism
- ORPHA:100090Rare parathyroid tumor
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/68415
- This record as JSON: /data/d/68415.json