{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0007767/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"endocrine system disorder",
"skeletal dysplasia",
"musculoskeletal system disorder",
"familial primary hyperparathyroidism",
"disease",
"connective tissue disease",
"human disease",
"endocrine gland neoplasm",
"hereditary neoplastic syndrome",
"musculoskeletal system disease",
"hereditary disorder of connective tissue",
"skeletal system disorder",
"experimental factor",
"entity",
"neoplastic disease or syndrome",
"parathyroid gland disorder",
"quality",
"genetic disorder",
"neoplasm",
"hereditary disease",
"bone neoplasm",
"abnormal mineralization disorder",
"inherited disease susceptibility",
"primary hyperparathyroidism",
"parathyroid disease",
"neoplastic syndrome",
"syndromic disease",
"bone disorder",
"continuant",
"connective tissue disorder",
"realizable",
"disposition",
"characteristic",
"hyperparathyroidism 1",
"bone disease",
"skeletal system disease",
"tumor of parathyroid gland",
"cancer or benign tumor",
"endocrine neoplasm",
"disease susceptibility",
"hyperparathyroidism",
"endocrine system disease",
"hereditary hyperparathyroidism",
"familial isolated hyperparathyroidism",
"connective tissue neoplasm"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:53:51.201287+00:00",
"name": "MONDO_0007767",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:40:27.261335+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "hyperparathyroidism 1",
"synonyms": [
"hyperparathyroidism type 1",
"hyperparathyroidism, familial primary",
"hyperparathyroidism 1"
],
"term_id": "MONDO:0007767",
"term_name": "hyperparathyroidism 1",
"uuid": "f79febb4-f4f3-4788-9cd3-f5f376732765"
}