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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Familial primary hyperparathyroidism | |
| Synonyms |
|
|
| ID |
http://www.orpha.net/ORDO/Orphanet_2207 |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=2207 |
|
| has_age_of_onset |
Childhood
|
|
| has_inheritance |
Autosomal dominant
|
|
| label |
Familial primary hyperparathyroidism
|
|
| notation |
Clinical group ORPHA:2207
|
|
| prefixIRI |
ORDO:Orphanet_2207
|
|
| prefLabel |
Familial primary hyperparathyroidism
|
|
| present_in |
Worldwide AND has_point_prevalence_range : Unknown
|
|
| subClassOf |
http://www.orpha.net/ORDO/Orphanet_208596 http://www.orpha.net/ORDO/Orphanet_100090 |
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