{
    "disease_id": "DOID:0060701",
    "recommended_name": {
        "id": "DOID:0060701",
        "resource": "Disease Ontology",
        "url": "http://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": "http://disease-ontology.org/term/DOID:0060701",
            "name": "FHH type 2",
            "description": ""
        },
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060701",
            "name": "HHC2",
            "description": ""
        },
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060701",
            "name": "familial hypocalciuric hypercalcemia type 2",
            "description": ""
        },
        {
            "id": "DOID:0060701",
            "resource": "Disease Ontology",
            "url": "http://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": "hypocalciuric hypercalcemia, familial, 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": "hypocalciuric hypercalcemia, familial, type 2",
            "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": "hypocalciuric hypercalcemia, familial, type II; HHC2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "familial benign hypercalcemia, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007792",
            "name": "hypocalciuric hypercalcemia type II",
            "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": "hypercalcemia, familial benign, type 2",
            "description": ""
        },
        {
            "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": "hypercalcemia, familial benign type 2",
            "description": ""
        },
        {
            "id": "MIM:145981",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/145981",
            "name": "Hypocalciuric hypercalcemia, familial 2",
            "description": "Hypocalciuric hypercalcemia, familial 2"
        }
    ]
}