{
	"id":"SAMS_export_2026-05-03",
	"subject":{
		"id":"75312656",
		"sex":"MALE"
	},
	"phenotypicFeatures":[
		{
			"type":{
				"id":"HP:0002612",
				"label":"Congenital hepatic fibrosis"
			},
			"onset":{
				"timestamp":"2024-08-16T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0000113",
				"label":"Polycystic kidney dysplasia"
			},
			"onset":{
				"timestamp":"2024-08-16T00:00:00Z"
			}
		}
	],
	"metaData":{
		"created":"2026-05-03T15:28:40Z",
		"createdBy":"?",
		"resources":[
			{
				"id":"hp",
				"name":"human phenotype ontology",
				"url":"http://purl.obolibrary.org/obo/hp.obo",
				"version":"2025-09-01",
				"namespacePrefix":"HP",
				"iriPrefix":"http://purl.obolibrary.org/obo/HP_"
			}
		],
		"phenopacketSchemaVersion":"2.0"
	}
}