{
    "disease_id": "DOID:0110050",
    "recommended_name": {
        "id": "DOID:0110050",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110050",
        "name": "Alzheimer's disease 18",
        "description": "An Alzheimer's disease that has_material_basis_in a mutation in the ADAM10 gene on chromosome 15q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110050",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110050",
            "name": "AD18",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110050",
            "name": "Alzheimer disease 18",
            "description": ""
        },
        {
            "id": "DOID:0110050",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110050",
            "name": "Alzheimer's disease 18, late onset",
            "description": ""
        },
        {
            "id": "MONDO:0014265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014265",
            "name": "Alzheimer disease 18",
            "description": "Any Alzheimer disease in which the cause of the disease is a mutation in the ADAM10 gene."
        },
        {
            "id": "MONDO:0014265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014265",
            "name": "AD18",
            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014265",
            "name": "ADAM10 Alzheimer disease",
            "description": ""
        },
        {
            "id": "MONDO:0014265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014265",
            "name": "Alzheimer disease 18",
            "description": ""
        },
        {
            "id": "MONDO:0014265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014265",
            "name": "Alzheimer disease caused by mutation in ADAM10",
            "description": ""
        },
        {
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            "resource": "MONDO",
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            "description": ""
        },
        {
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            "resource": "MONDO",
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            "description": ""
        },
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            "description": ""
        },
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/615590",
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            "description": "Alzheimer disease 18"
        }
    ],
    "children": [],
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        "DOID:0110050"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0110050",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110050",
            "categories": []
        },
        {
            "id": "MONDO:0014265",
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            "categories": []
        },
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            "url": "https://www.omim.org/entry/615590",
            "categories": []
        }
    ],
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            "uniprot_ac": "A0A1D5NT24",
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                    "type": "recommended"
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                }
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                    "name": "Madm",
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                    "name": "ADAM10",
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                    "name": "AD10",
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                    "name": "AD18",
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                    "name": "ADAM10",
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                    "name": "CD156c",
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                    "name": "CDw156",
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                    "name": "HsT18717",
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                    "name": "KUZ",
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                    "name": "RAK",
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                    "id": "0110050",
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                    "name": "ADAM10 endopeptidase",
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            ],
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                    "name": "Senescence-associated epithelial membrane protein",
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                    "name": "claudin-1",
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    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110050"
}
