{
    "disease_id": "DOID:0111154", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "orthostatic intolerance due to NET deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "orthostatic intolerance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "postural tachycardia syndrome due to NET deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "soldiers heart"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "mitral valve prolapse syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "familial orthostatic tachycardia due to norepinephrine transporter deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "orhtostatic intolerance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "irritable heart"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011479", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011479", 
            "name": "neurocirculatory asthenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "irritable heart"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "mitral valve prolapse syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "neurocirculatory asthenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "orhtostatic intolerance"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "orthostatic intolerance due to NET deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "soldiers heart"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "postural tachycardia syndrome due to NET deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111154", 
            "name": "familial orthostatic tachycardia due to norepinephrine transporter deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/604715", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:604715", 
            "name": "Orthostatic intolerance"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111154", 
        "description": "A heart conduction disease characterized by orthostatic intolerance that has_material_basis_in heterozygous mutation in the SLC6A2 gene on chromosome 16q12.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111154", 
        "name": "postural orthostatic tachycardia syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/604715", 
            "id": "604715", 
            "database": "MIM"
        }
    ]
}
