{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0007767/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"endocrine gland neoplasm",
"familial primary hyperparathyroidism",
"entity",
"neoplastic syndrome",
"bone disease",
"inherited disease susceptibility",
"hereditary disease",
"skeletal system disease",
"musculoskeletal system disorder",
"endocrine system disorder",
"hyperparathyroidism 1",
"experimental factor",
"disposition",
"familial isolated hyperparathyroidism",
"connective tissue disorder",
"tumor of parathyroid gland",
"cancer or benign tumor",
"endocrine neoplasm",
"continuant",
"neoplasm",
"hyperparathyroidism",
"hereditary hyperparathyroidism",
"human disease",
"musculoskeletal system disease",
"characteristic",
"skeletal system disorder",
"bone neoplasm",
"hereditary disorder of connective tissue",
"neoplastic disease or syndrome",
"bone disorder",
"disease susceptibility",
"endocrine system disease",
"syndromic disease",
"connective tissue neoplasm",
"genetic disorder",
"realizable",
"quality",
"skeletal dysplasia",
"disease",
"parathyroid gland disorder",
"connective tissue disease",
"abnormal mineralization disorder",
"parathyroid disease",
"hereditary neoplastic syndrome",
"primary hyperparathyroidism"
],
"audit": {},
"comments": [],
"creation_timestamp": "2023-11-03T21:53:51.201287+00:00",
"definition": "",
"name": "MONDO_0007767",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:40:27.261335+00:00",
"schema_version": "5",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "hyperparathyroidism 1",
"synonyms": [
"hyperparathyroidism type 1",
"hyperparathyroidism 1",
"hyperparathyroidism, familial primary"
],
"term_id": "MONDO:0007767",
"term_name": "hyperparathyroidism 1",
"uuid": "f79febb4-f4f3-4788-9cd3-f5f376732765"
}