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Cell Culture Ontology
Last uploaded:
July 23, 2014
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| Id | http://purl.obolibrary.org/obo/MONDO_0016365
http://purl.obolibrary.org/obo/MONDO_0016365
|
|---|---|
| Preferred Name | familial primary hyperparathyroidism |
| Definitions |
An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome.
|
| Synonyms |
hereditary primary hyperparathyroidism (disease)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome. |
|---|---|
| preferred label | familial primary hyperparathyroidism
|
| label | familial primary hyperparathyroidism
|
| prefLabel | familial primary hyperparathyroidism
|
| database_cross_reference |
UMLS:C0271846
icd11.foundation:1186866066
Orphanet:2207
MEDGEN:543605
GARD:2837
|
| notation | MONDO:0016365
|
| in_subset | |
| id | MONDO:0016365
|
| skos_exactMatch | |
| subClassOf | |
| type | |
| has_exact_synonym | hereditary primary hyperparathyroidism (disease)
|
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