{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009992", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009992", 
            "name": "myoglobinuria, acute recurrent, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009992", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009992", 
            "name": "myoglobinuria, familial paroxysmal paralytic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009992", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009992", 
            "name": "rhabdomyolysis, acute recurrent"
        }, 
        {
            "url": "https://www.omim.org/entry/268200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:268200", 
            "name": "Myoglobinuria, acute recurrent, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080108", 
        "description": "A myopathy that is characterized by an increased urinary excretion of myoglobin.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080108", 
        "name": "myoglobinuria"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/268200", 
            "id": "268200", 
            "database": "MIM"
        }
    ]
}