{
"description": "Example value set for Condition/Problem/Diagnosis codes.",
"compose": {
"include": [ {
"filter": [ {
"op": "is-a",
"value": "404684003",
"property": "concept"
} ],
"system": "http://snomed.info/sct"
}, {
"system": "http://snomed.info/sct",
"concept": [ {
"code": "160245001",
"display": "No current problems or disability"
} ]
} ]
},
"_filename": "ValueSet-condition-code.json",
"package_name": "hl7.fhir.r6.expansions",
"date": null,
"meta": {
"lastUpdated": "2025-12-18T07:07:42.170+11:00"
},
"publisher": "FHIR Project team",
"jurisdiction": [ {
"coding": [ {
"code": "001",
"system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
"display": "World"
} ]
} ],
"name": "ConditionProblemDiagnosisCodes",
"copyright": "This resource includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these specifications must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/get-snomed-ct or info@snomed.org",
"type": null,
"experimental": "false",
"resourceType": "ValueSet",
"expansion": {
"offset": 0,
"contains": [ {
"code": "404684003",
"system": "http://snomed.info/sct",
"display": "Clinical finding (finding)",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Clinical finding",
"language": "en"
} ]
}, {
"code": "109006",
"system": "http://snomed.info/sct",
"display": "Anxiety disorder of childhood OR adolescence",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Anxiety disorder of childhood or adolescence, NOS",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Anxiety disorder of childhood OR adolescence (disorder)",
"language": "en"
} ]
}, {
"code": "122003",
"system": "http://snomed.info/sct",
"display": "Choroidal hemorrhage",
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"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Choroidal hemorrhage, NOS",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Choroidal haemorrhage",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Choroidal hemorrhage (disorder)",
"language": "en"
} ]
}, {
"code": "127009",
"system": "http://snomed.info/sct",
"display": "Spontaneous abortion with laceration of cervix",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Spontaneous abortion with tear of cervix",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Spontaneous abortion with laceration of cervix (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Miscarriage with tear of cervix",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Miscarriage with laceration of cervix",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Miscarriage with laceration of cervix (disorder)",
"language": "en"
} ]
}, {
"code": "129007",
"system": "http://snomed.info/sct",
"display": "Homoiothermia",
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"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Homoiothermy",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Homoiothermia (finding)",
"language": "en"
} ]
}, {
"code": "134006",
"system": "http://snomed.info/sct",
"display": "Decreased hair growth",
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"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Decreased hair growth function",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Decreased hair growth (finding)",
"language": "en"
} ]
}, {
"code": "140004",
"system": "http://snomed.info/sct",
"display": "Chronic pharyngitis",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Chronic sore throat",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Chronic pharyngitis (disorder)",
"language": "en"
} ]
}, {
"code": "144008",
"system": "http://snomed.info/sct",
"display": "Normal peripheral vision",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Normal peripheral vision (finding)",
"language": "en"
} ]
}, {
"code": "150003",
"system": "http://snomed.info/sct",
"display": "Abnormal bladder continence",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Abnormal bladder continence (finding)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Abnormal urinary bladder continence",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Abnormal urinary bladder continence (finding)",
"language": "en"
} ]
}, {
"code": "151004",
"system": "http://snomed.info/sct",
"display": "Gonococcal meningitis",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Gonococcal meningitis (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Meningitis due to gonococcus",
"language": "en"
} ]
}, {
"code": "162004",
"system": "http://snomed.info/sct",
"display": "Severe manic bipolar I disorder without psychotic features",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Severe bipolar I disorder, most recent episode manic, without psychotic features",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Severe manic bipolar disorder without psychotic features",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Severe manic bipolar I disorder without psychotic features (disorder)",
"language": "en"
} ]
}, {
"code": "165002",
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"display": "Accident-prone",
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"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Accident-prone behavior",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Accident proneness",
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}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Accident prone",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Accident prone (finding)",
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} ]
}, {
"code": "168000",
"system": "http://snomed.info/sct",
"display": "Typhlolithiasis",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Typhlolithiasis (disorder)",
"language": "en"
} ]
}, {
"code": "171008",
"system": "http://snomed.info/sct",
"display": "Injury of ascending right colon without open wound into abdominal cavity",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Injury of ascending right colon without open wound into abdominal cavity (disorder)",
"language": "en"
} ]
}, {
"code": "175004",
"system": "http://snomed.info/sct",
"display": "Supraorbital neuralgia",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Supraorbital neuralgia (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Supraorbital neuralgia (finding)",
"language": "en"
} ]
}, {
"code": "177007",
"system": "http://snomed.info/sct",
"display": "Poisoning by sawfly larvae",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Sawfly larvae toxicity",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Poisoning by sawfly larvae (disorder)",
"language": "en"
} ]
}, {
"code": "179005",
"system": "http://snomed.info/sct",
"display": "Apraxia of dressing",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Apraxia of dressing (finding)",
"language": "en"
} ]
}, {
"code": "181007",
"system": "http://snomed.info/sct",
"display": "Hemorrhagic bronchopneumonia",
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"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Haemorrhagic bronchopneumonia",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Hemorrhagic bronchopneumonia (disorder)",
"language": "en"
} ]
}, {
"code": "183005",
"system": "http://snomed.info/sct",
"display": "Autoimmune pancytopenia",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Autoimmune pancytopenia (disorder)",
"language": "en"
} ]
}, {
"code": "184004",
"system": "http://snomed.info/sct",
"display": "Withdrawal arrhythmia",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Withdrawal arrhythmia (disorder)",
"language": "en"
} ]
}, {
"code": "188001",
"system": "http://snomed.info/sct",
"display": "Injury of intercostal artery",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Injury of intercostal artery (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Intercostal artery injury",
"language": "en"
} ]
}, {
"code": "192008",
"system": "http://snomed.info/sct",
"display": "Congenital syphilitic hepatomegaly",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Congenital syphilitic hepatomegaly (disorder)",
"language": "en"
} ]
}, {
"code": "193003",
"system": "http://snomed.info/sct",
"display": "Benign hypertensive renal disease",
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"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Benign hypertensive renal disease (disorder)",
"language": "en"
} ]
}, {
"code": "198007",
"system": "http://snomed.info/sct",
"display": "Disease caused by Filoviridae (disorder)",
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"use": {
"code": "900000000000546006",
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"display": "Inactive value"
},
"value": "Disease due to Filovirus",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Disease due to Filovirus, NOS",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Disease due to Filovirus (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Disease due to Filoviridae (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Disease due to Filoviridae",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Disease caused by Filoviridae",
"language": "en"
} ]
}, {
"code": "199004",
"system": "http://snomed.info/sct",
"display": "Decreased lactation",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hypogalactia",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hypolactation",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Insufficient lactation",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Poor lactation",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Inadequate lactation",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Decreased lactation (finding)",
"language": "en"
} ]
}, {
"code": "216004",
"system": "http://snomed.info/sct",
"display": "Delusion of persecution",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Paranoid delusion",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Paranoid reaction",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Persecutory delusion",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Delusion of persecution (finding)",
"language": "en"
} ]
}, {
"code": "219006",
"system": "http://snomed.info/sct",
"display": "Alcohol user",
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"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Alcoholic beverage drinker",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Alcoholic beverage drinker, NOS",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
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"value": "Current drinker",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
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"value": "Drinks alcohol",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Current drinker (life style)",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Current drinker of alcohol (finding)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Current drinker of alcohol",
"language": "en"
} ]
}, {
"code": "222008",
"system": "http://snomed.info/sct",
"display": "Acute epiglottitis with obstruction",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Acute epiglottitis with obstruction (disorder)",
"language": "en"
} ]
}, {
"code": "223003",
"system": "http://snomed.info/sct",
"display": "Tumor of body of uterus affecting pregnancy",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tumour of body of uterus affecting pregnancy",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Tumor of body of uterus affecting pregnancy (disorder)",
"language": "en"
} ]
}, {
"code": "228007",
"system": "http://snomed.info/sct",
"display": "Lucio phenomenon",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Lepromatous cutaneous vasculitis",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Lucio phenomenon (disorder)",
"language": "en"
} ]
}, {
"code": "241006",
"system": "http://snomed.info/sct",
"display": "Epilepsia partialis continua",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Kojevnikov's epilepsy",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Epilepsia partialis continua (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Motor simple partial status",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Kojewnikov's epilepsy",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Focal status epilepticus",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Kojevnikov epilepsy",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Epilepsia partialis continua (finding)",
"language": "en"
}, {
"use": {
"code": "900000000000550004",
"system": "http://snomed.info/sct",
"display": "Definition"
},
"value": "A prolonged focal-onset clonic seizure occurring and limited to specific parts of the body such as the hand, face, arm or leg.",
"language": "en"
} ]
}, {
"code": "242004",
"system": "http://snomed.info/sct",
"display": "Noninfectious jejunitis",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
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"use": {
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"value": "Altered blood passed per rectum",
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"value": "Altered blood in stool",
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"value": "Brachial plexus disorder",
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"value": "Brachial neuritis",
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"value": "Neuralgic amyotrophy",
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"value": "Thyromegaly",
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"value": "Goitre, NOS",
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"value": "Goitre",
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}, {
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"value": "Swelling of thyroid gland",
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"value": "Thyroid enlargement",
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}, {
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"value": "Congenital duplication of intestine (disorder)",
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}, {
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"value": "Disease of pancreas (disorder)",
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"use": {
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"value": "Disorder of pancreas (disorder)",
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} ]
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"value": "ABO isoimmunisation affecting pregnancy",
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"value": "ABO isoimmunization affecting pregnancy (disorder)",
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"use": {
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"value": "ABO isoimmunisation in pregnancy",
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}, {
"use": {
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"display": "Synonym (core metadata concept)"
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"value": "ABO isoimmunization in pregnancy",
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} ]
}, {
"code": "3886001",
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"display": "Congenital fecaliths",
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"value": "Congenital faecaliths",
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"use": {
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"value": "Congenital fecaliths (disorder)",
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} ]
}, {
"code": "3899003",
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"display": "Neutropenic typhlitis",
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"value": "Neutropenic typhlitis (disorder)",
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"value": "Fleckenkrankheit",
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}, {
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"value": "Infection by Nosema bombycis (disorder)",
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}, {
"use": {
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"value": "Pébrine",
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}, {
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"value": "Pebrine",
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}, {
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},
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}, {
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} ]
}, {
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} ]
}, {
"code": "4846001",
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"display": "Anicteric viral hepatitis",
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} ]
}, {
"code": "4851007",
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}, {
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} ]
}, {
"code": "4853005",
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} ]
}, {
"code": "4854004",
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"display": "Acquired hemolytic anemia",
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} ]
}, {
"code": "4855003",
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}, {
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}, {
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}, {
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"value": "DR - Diabetic retinopathy",
"language": "en"
}, {
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"value": "DR",
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}, {
"use": {
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},
"value": "Retinopathy co-occurrent and due to diabetes mellitus (disorder)",
"language": "en"
}, {
"use": {
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"display": "Inactive value"
},
"value": "Retinopathy co-occurrent and due to diabetes mellitus",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Retinopathy due to diabetes mellitus",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Retinopathy due to diabetes mellitus (disorder)",
"language": "en"
} ]
}, {
"code": "4859009",
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"display": "Lichen spinulosus",
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},
"value": "Lichen spinulosus (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Keratosis spinulosa",
"language": "en"
} ]
}, {
"code": "4860004",
"system": "http://snomed.info/sct",
"display": "Infection by Aspergillus niger",
"designation": [ {
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"value": "Infection by Aspergillus niger (disorder)",
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}, {
"use": {
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"display": "Synonym (core metadata concept)"
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"value": "Infection caused by Aspergillus niger",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
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"display": "Fully specified name"
},
"value": "Infection caused by Aspergillus niger (disorder)",
"language": "en"
} ]
}, {
"code": "4863002",
"system": "http://snomed.info/sct",
"display": "Phencyclidine-induced mood disorder",
"designation": [ {
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"value": "PCP mood disorder",
"language": "en"
}, {
"use": {
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"value": "PCP mood disorder (disorder)",
"language": "en"
}, {
"use": {
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"display": "Inactive value"
},
"value": "Phencyclidine (PCP) mood disorder (disorder)",
"language": "en"
}, {
"use": {
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"display": "Inactive value"
},
"value": "Phencyclidine (PCP) mood disorder",
"language": "en"
}, {
"use": {
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"display": "Synonym (core metadata concept)"
},
"value": "Phencyclidine mood disorder",
"language": "en"
}, {
"use": {
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"display": "Inactive value"
},
"value": "Phencyclidine mood disorder (disorder)",
"language": "en"
}, {
"use": {
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"value": "PCP induced mood disorder",
"language": "en"
}, {
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"display": "Synonym (core metadata concept)"
},
"value": "PCP (phencyclidine) mood disorder",
"language": "en"
}, {
"use": {
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"display": "Fully specified name"
},
"value": "Mood disorder caused by phencyclidine (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Mood disorder caused by phencyclidine",
"language": "en"
} ]
}, {
"code": "4873000",
"system": "http://snomed.info/sct",
"display": "Localized vascularization of cornea",
"designation": [ {
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"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Localised vascularisation of cornea",
"language": "en"
}, {
"use": {
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"display": "Fully specified name"
},
"value": "Localized vascularization of cornea (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
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"display": "Synonym (core metadata concept)"
},
"value": "Localised corneal vascularisation",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Localized corneal vascularization",
"language": "en"
} ]
}, {
"code": "4874006",
"system": "http://snomed.info/sct",
"display": "11q partial trisomy syndrome",
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"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "11q partial trisomy syndrome (disorder)",
"language": "en"
} ]
}, {
"code": "4886009",
"system": "http://snomed.info/sct",
"display": "Premature birth of newborn male",
"designation": [ {
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},
"value": "Premature male newborn",
"language": "en"
}, {
"use": {
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"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Premature birth of newborn male (finding)",
"language": "en"
} ]
}, {
"code": "4887000",
"system": "http://snomed.info/sct",
"display": "Hypertyrosinemia, Richner-Hanhart type",
"designation": [ {
"use": {
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"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosine transaminase deficiency",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Oculocutaneous tyrosinemia",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Richner-Hanhart syndrome",
"language": "en"
}, {
"use": {
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"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Tyrosinemia, type II",
"language": "en"
}, {
"use": {
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"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hereditary hypertyrosinemia, type II",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hypertyrosinemia, Oregon type",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Keratosis palmoplantaris with corneal dystrophy",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Persistent hypertyrosinemia",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Richner syndrome",
"language": "en"
}, {
"use": {
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"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinemia without hepatorenal dysfunction",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hereditary hypertyrosinaemia, type II",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hypertyrosinaemia, Oregon type",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinemia type II",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Oculocutaneous tyrosinaemia",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinaemia type II",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Hypertyrosinaemia, Richner-Hanhart type",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Persistent hypertyrosinaemia",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinaemia without hepatorenal dysfunction",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Tyrosinaemia, type II",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Hypertyrosinemia, Richner-Hanhart type (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinaemia type 2",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinemia type 2",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinaemia due to tyrosine aminotransferase deficiency",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Tyrosinemia due to tyrosine aminotransferase deficiency",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "TAT-gene related hypertyrosinemia Richner Hanhart type",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "TAT-gene related hypertyrosinaemia Richner Hanhart type",
"language": "en"
}, {
"use": {
"code": "900000000000550004",
"system": "http://snomed.info/sct",
"display": "Definition"
},
"value": "An inborn error of tyrosine metabolism characterized by hypertyrosinemia with oculocutaneous manifestations and in some cases intellectual deficit. Skin lesions occur in 80% of cases, ocular involvement in 75% of cases and neurologic findings and some degree of intellectual deficit in up to 60% of cases. Onset is variable but the ocular symptoms (redness, photophobia, excessive tearing and pain) usually develop in the first year of life. Cutaneous manifestations usually begin after the first year of life but may develop at the same time as the ocular symptoms. Caused by mutations in the TAT gene (16q22.1) encoding tyrosine aminotransferase (TAT). The elevated levels of tyrosine caused by TAT deficiency appear to result in deposition of tyrosine crystals leading to an inflammatory response and the oculocutaneous findings. Transmitted as an autosomal recessive trait.",
"language": "en"
}, {
"use": {
"code": "900000000000550004",
"system": "http://snomed.info/sct",
"display": "Definition"
},
"value": "An inborn error of tyrosine metabolism characterised by hypertyrosinaemia with oculocutaneous manifestations and in some cases intellectual deficit. Skin lesions occur in 80% of cases, ocular involvement in 75% of cases and neurologic findings and some degree of intellectual deficit in up to 60% of cases. Onset is variable but the ocular symptoms (redness, photophobia, excessive tearing and pain) usually develop in the first year of life. Cutaneous manifestations usually begin after the first year of life but may develop at the same time as the ocular symptoms. Caused by mutations in the TAT gene (16q22.1) encoding tyrosine aminotransferase (TAT). The elevated levels of tyrosine caused by TAT deficiency appear to result in deposition of tyrosine crystals leading to an inflammatory response and the oculocutaneous findings. Transmitted as an autosomal recessive trait.",
"language": "en"
} ]
}, {
"code": "4896000",
"system": "http://snomed.info/sct",
"display": "Acute toxic hepatitis",
"designation": [ {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Acute toxic hepatitis (disorder)",
"language": "en"
} ]
}, {
"code": "4900002",
"system": "http://snomed.info/sct",
"display": "Endocrine disorder related to puberty",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Endocrine disorder related to puberty, NOS",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Endocrine disorder related to puberty (disorder)",
"language": "en"
} ]
}, {
"code": "4907004",
"system": "http://snomed.info/sct",
"display": "Non-involution of uterus",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Failure of involution of uterus",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Non-involution of uterus (disorder)",
"language": "en"
} ]
}, {
"code": "4915001",
"system": "http://snomed.info/sct",
"display": "Infection by Entamoeba coli",
"designation": [ {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Entamebiasis coli",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Entamoebosis coli",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Entamoebiasis coli",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Infection by Entameba coli",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Infection by Entamoeba coli (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Infection caused by Entamoeba coli (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Infection caused by Entamoeba coli",
"language": "en"
} ]
}, {
"code": "4920001",
"system": "http://snomed.info/sct",
"display": "Deficiency of acetyl-CoA carboxylase",
"designation": [ {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Acetyl-CoA: carboxylase deficiency",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "ACC deficiency",
"language": "en"
}, {
"use": {
"code": "900000000000546006",
"system": "http://snomed.info/sct",
"display": "Inactive value"
},
"value": "Acetyl-CoA: carboxylase deficiency (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000003001",
"system": "http://snomed.info/sct",
"display": "Fully specified name"
},
"value": "Deficiency of acetyl-coenzyme A carboxylase (disorder)",
"language": "en"
}, {
"use": {
"code": "900000000000013009",
"system": "http://snomed.info/sct",
"display": "Synonym (core metadata concept)"
},
"value": "Acetyl-CoA carboxylase deficiency",
"language": "en"
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"value": "urn:oid:2.16.840.1.113883.4.642.3.152",
"system": "urn:ietf:rfc:3986"
}, {
"use": "old",
"value": "urn:oid:2.16.840.1.113883.4.642.2.72",
"system": "urn:ietf:rfc:3986"
} ],
"version": "6.0.0-ballot4",
"contact": [ {
"telecom": [ {
"value": "http://hl7.org/fhir",
"system": "url"
} ]
} ]
}