{
    "disease_id": "DOID:0090045", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "ped"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "paroxysmal exercise-induced dystonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "GLUT1 deficiency syndrome 2; GLUT1DS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "GLUT1 deficiency syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "GLUT1DS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "GLUT1 deficiency syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "dystonia 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "childhood onset GLUT1 deficiency syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "ped with or without epilepsy and/or hemolytic Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "DYT18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "paroxysmal exertion-induced dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "DYT-SLC2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012805", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012805", 
            "name": "PxMD-SLC2A1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090045", 
        "description": "A dystonia that is characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090045", 
        "name": "childhood onset GLUT1 deficiency syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090045#disease-associations", 
            "id": "0090045", 
            "database": "Alliance of Genome Resources"
        }
    ]
}