{
    "disease_id": "DOID:0060702",
    "recommended_name": {
        "id": "DOID:0060702",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060702",
        "name": "familial hypocalciuric hypercalcemia 3",
        "description": "A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the AP2S1 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0060702",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060702",
            "name": "FHH type 3",
            "description": ""
        },
        {
            "id": "DOID:0060702",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060702",
            "name": "HHC3",
            "description": ""
        },
        {
            "id": "DOID:0060702",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060702",
            "name": "familial hypocalciuric hypercalcemia type 3",
            "description": ""
        },
        {
            "id": "DOID:0060702",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060702",
            "name": "hypocalciuric hypercalcemia type III",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "familial hypocalciuric hypercalcemia 3",
            "description": "Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the AP2S1 gene."
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypercalcemia, familial benign, Oklahoma type",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "FHH type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "familial benign hypercalcemia, Oklahoma variant",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "familial benign hypercalcemia, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "familial hypocalciuric hypercalcemia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypocalciuric hypercalcemia type III",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "FBHOk",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "FBH3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypercalcemia, familial benign, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypocalciuric hypercalcemia, familial, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "HHC3",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypocalciuric hypercalcemia, familial, type III",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "AP2S1 familial hypocalciuric hypercalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "familial hypocalciuric hypercalcemia caused by mutation in AP2S1",
            "description": ""
        },
        {
            "id": "MONDO:0010926",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010926",
            "name": "hypocalciuric hypercalcemia, familial, type III; HHC3",
            "description": ""
        },
        {
            "id": "MIM:600740",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600740",
            "name": "Hypocalciuric hypercalcemia, familial 3",
            "description": "Hypocalciuric hypercalcemia, familial 3"
        }
    ]
}