{
	"id":"SAMS_export_2026-05-03",
	"subject":{
		"id":"XYZ007",
		"sex":"FEMALE"
	},
	"phenotypicFeatures":[
		{
			"modifiers":[
				{
					"id":"HP:0012824",
					"label":"Severity"
				}
			],
			"type":{
				"id":"HP:0030261",
				"label":"Absent penis"
			},
			"onset":{
				"timestamp":"2026-02-11T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0011025",
				"label":"Abnormal cardiovascular system physiology"
			},
			"onset":{
				"timestamp":"2022-07-03T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0001919",
				"label":"Acute kidney injury"
			},
			"onset":{
				"timestamp":"2022-07-02T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0012211",
				"label":"Abnormal renal physiology"
			},
			"onset":{
				"timestamp":"2022-07-01T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0001919",
				"label":"Acute kidney injury"
			},
			"onset":{
				"timestamp":"2022-06-29T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0000790",
				"label":"Hematuria"
			},
			"onset":{
				"timestamp":"2022-06-29T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0000124",
				"label":"Renal tubular dysfunction"
			},
			"onset":{
				"timestamp":"2022-06-29T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0100817",
				"label":"Renovascular hypertension"
			},
			"onset":{
				"timestamp":"2022-06-29T00:00:00Z"
			}
		},
		{
			"type":{
				"id":"HP:0001945",
				"label":"Fever"
			},
			"onset":{
				"timestamp":"2022-06-26T00:00:00Z"
			},
			"excluded":true
		},
		{
			"type":{
				"id":"HP:0000790",
				"label":"Hematuria"
			},
			"onset":{
				"timestamp":"2022-06-26T00:00:00Z"
			}
		}
	],
	"diseases":[
		{
			"term":{
				"id":"ORPHA:2072",
				"label":"Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome"
			},
			"onset":{
				"timestamp":"2022-07-03T00:00:00Z"
			}
		},
		{
			"term":{
				"id":"ORPHA:730",
				"label":"Autosomal dominant polycystic kidney disease"
			},
			"onset":{
				"timestamp":"2022-06-29T00:00:00Z"
			}
		}
	],
	"metaData":{
		"created":"2026-05-03T13:28:40Z",
		"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_"
			},
			{
				"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"
	}
}