{
    "disease_id": "DOID:0060651", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "May-Hegglin anomaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "MHA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "Dohle leukocyte inclusions with giant platelets"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "matins"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "macrothrombocytopenia with leukocyte inclusions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "bleeding disorder, Platelet-type, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "May-Hegglin thrombocytopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss; matins"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "MAY-Hegglin anomaly; MHA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007954", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007954", 
            "name": "macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss"
        }, 
        {
            "url": "https://www.omim.org/entry/155100", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:155100", 
            "name": "Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060651", 
        "description": "A blood platelet disease that has_material_basis_in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060651", 
        "name": "MYH-9 related disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/155100", 
            "id": "155100", 
            "database": "MIM"
        }
    ]
}