{
	"id":"SAMS_export_2026-05-03",
	"subject":{
		"id":"testpat2",
		"sex":"MALE"
	},
	"phenotypicFeatures":[
		{
			"type":{
				"id":"HP:0011400",
				"label":"Abnormal CNS myelination"
			},
			"onset":{
				"timestamp":"2025-07-03T00:00:00Z"
			}
		},
		{
			"modifiers":[
				{
					"id":"HP:4000120",
					"label":"Triggered by nickel"
				}
			],
			"type":{
				"id":"HP:0033836",
				"label":"Abnormal intrarenal artery morphology"
			},
			"onset":{
				"timestamp":"2022-05-06T00:00:00Z"
			}
		}
	],
	"diseases":[
		{
			"term":{
				"id":"ORPHA:122",
				"label":"Birt-Hogg-Dubé syndrome"
			},
			"onset":{
				"timestamp":"2022-05-05T00:00:00Z"
			}
		}
	],
	"metaData":{
		"created":"2026-05-03T15:23:59Z",
		"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_"
			},
			{
				"id":"orphanet",
				"name":"orphanet rare disease ontology",
				"url":"http://www.orpha.net",
				"version":"2025-06-24 07:31:42",
				"namespacePrefix":"ORPHA",
				"iriPrefix":"https://www.orpha.net/en/disease/detail/"
			}
		],
		"phenopacketSchemaVersion":"2.0"
	}
}