{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0015967/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"aliases": [
"kyle-gaulton:phenotype_monogenicDiabetes"
],
"ancestors": [
"specifically dependent continuant",
"endocrine system disorder",
"experimental factor",
"realizable entity",
"genetic disorder",
"pancreas disease",
"monogenic diabetes",
"glucose metabolism disease",
"entity",
"digestive system disorder",
"disposition",
"metabolic disease",
"continuant",
"pancreas disorder",
"diabetes mellitus",
"digestive system disease",
"endocrine system disease",
"inborn errors of metabolism",
"disease",
"hereditary disease",
"endocrine pancreas disorder",
"human disease"
],
"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": [
"monogenic diabetes",
"rare genetic diabetes mellitus"
],
"term_id": "MONDO:0015967",
"term_name": "monogenic diabetes",
"uuid": "7486f60c-707a-4d19-8b9f-6efcd0b9957d"
}