{
    "disease_id": "DOID:0060651",
    "recommended_name": {
        "id": "DOID:0060651",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060651",
        "name": "MYH-9 related disease",
        "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."
    },
    "synonyms": [
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        },
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            "name": "MHA",
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        },
        {
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            "name": "MYH9-related disease",
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            "name": "MYH9-related disorder",
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        {
            "id": "MONDO:0015912",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015912",
            "name": "MYH9 related thrombocytopenia",
            "description": ""
        },
        {
            "id": "MIM:155100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/155100",
            "name": "Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss",
            "description": "Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060651"
    ],
    "unlinked_id_list": []
}