{
    "disease_id": "DOID:0060702", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypercalcemia, familial benign, Oklahoma type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "FHH type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "familial benign hypercalcemia, Oklahoma variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "familial benign hypercalcemia, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "familial hypocalciuric hypercalcemia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypocalciuric hypercalcemia type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "FBHOk"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "FBH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypercalcemia, familial benign, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypocalciuric hypercalcemia, familial, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "HHC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypocalciuric hypercalcemia, familial, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "AP2S1 familial hypocalciuric hypercalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "familial hypocalciuric hypercalcemia caused by mutation in AP2S1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010926", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010926", 
            "name": "hypocalciuric hypercalcemia, familial, type III; HHC3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060702", 
            "name": "FHH type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060702", 
            "name": "HHC3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060702", 
            "name": "familial hypocalciuric hypercalcemia type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060702", 
            "name": "hypocalciuric hypercalcemia type III"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060702", 
        "description": "A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the AP2S1 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060702", 
        "name": "familial hypocalciuric hypercalcemia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060702#disease-associations", 
            "id": "0060702", 
            "database": "Alliance of Genome Resources"
        }
    ]
}