{
    "disease_id": "DOID:0050635", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "alternating hemiplegia of childhood 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "alternating hemiplegia of childhood 1; AHC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "AHC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "alternating hemiplegia of childhood type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "ATP1A2 alternating hemiplegia of childhood"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007087", 
            "name": "alternating hemiplegia of childhood caused by mutation in ATP1A2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050635", 
            "name": "AHC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050635", 
        "description": "A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050635", 
        "name": "alternating hemiplegia of childhood"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050635#disease-associations", 
            "id": "0050635", 
            "database": "Alliance of Genome Resources"
        }
    ]
}