{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0015967/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"aliases": [
"kyle-gaulton:phenotype_monogenicDiabetes"
],
"ancestors": [
"disposition",
"glucose metabolism disease",
"pancreas disease",
"hereditary disease",
"metabolic disease",
"endocrine system disease",
"experimental factor",
"genetic disorder",
"monogenic diabetes",
"pancreas disorder",
"continuant",
"disease",
"human disease",
"endocrine pancreas disorder",
"digestive system disease",
"specifically dependent continuant",
"entity",
"inborn errors of metabolism",
"endocrine system disorder",
"realizable entity",
"diabetes mellitus",
"digestive system disorder"
],
"audit": {},
"creation_timestamp": "2024-12-04T00:06:41.445477+00:00",
"description": "Diabetes mellitus that is caused by mutations in a single gene.",
"name": "MONDO_0015967",
"ontology": "MONDO",
"release_timestamp": "2025-01-10T04:16:55.563147+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/5e3038c4-baa5-4589-b3d8-ad2fe634e826/",
"title": "Ying Sun"
},
"submitter_comment": "MONDO term",
"summary": "monogenic diabetes",
"synonyms": [
"rare genetic diabetes mellitus",
"monogenic diabetes"
],
"term_id": "MONDO:0015967",
"term_name": "monogenic diabetes",
"uuid": "7486f60c-707a-4d19-8b9f-6efcd0b9957d"
}