loading...| Preferred Name | familial primary hyperparathyroidism | |
| Synonyms |
hereditary primary hyperparathyroidism (disease) |
|
| Definitions |
An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0016365 |
|
| database_cross_reference |
UMLS:C0271846 icd11.foundation:1186866066 Orphanet:2207 MEDGEN:543605 GARD:2837 |
|
| definition |
An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome. |
|
| exactMatch |
http://identifiers.org/medgen/543605 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1186866066 |
|
| has_exact_synonym |
hereditary primary hyperparathyroidism (disease) |
|
| id |
MONDO:0016365 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping |
|
| label |
familial primary hyperparathyroidism |
|
| notation |
MONDO:0016365 |
|
| preferred label |
familial primary hyperparathyroidism |
|
| prefLabel |
familial primary hyperparathyroidism |
|
| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0016166 |