{
    "disease_id": "DOID:0060701",
    "recommended_name": {
        "id": "DOID:0060701",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060701",
        "name": "familial hypocalciuric hypercalcemia 2",
        "description": "A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060701",
            "name": "FHH type 2",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060701",
            "name": "HHC2",
            "description": ""
        },
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060701",
            "name": "familial hypocalciuric hypercalcemia type 2",
            "description": ""
        },
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060701",
            "name": "hypocalciuric hypercalcemia type II",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "familial hypocalciuric hypercalcemia 2",
            "description": "A familial hypocalciuric hypercalcemia that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13."
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "FHH type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "HHC2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "familial hypocalciuric hypercalcemia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "hpocalciuric hypercalcemia, type II",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "FBH2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "hypercalcemia, familial benign type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "hypocalciuric hypercalcemia, familial, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "hypocalciuric hypercalcemia, familial, type II",
            "description": ""
        },
        {
            "id": "MIM:145981",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/145981",
            "name": "Hypocalciuric hypercalcemia, familial 2",
            "description": "Hypocalciuric hypercalcemia, familial 2"
        }
    ],
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    "id_list": [
        "DOID:0060701"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0060701",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060701",
            "categories": []
        },
        {
            "id": "MONDO:0007792",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "categories": []
        },
        {
            "id": "MIM:145981",
            "database": "MIM",
            "url": "https://www.omim.org/entry/145981",
            "categories": []
        }
    ],
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        {
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            "uniprot_ac": "A0A0R4IEQ0",
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                    "name": "gna11a",
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            ],
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                    "name": "HG1K",
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                    "name": "DAC1",
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                    "id": "0060701",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060701"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0060701"
}