{
    "disease_id": "DOID:0060701", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypocalciuric hypercalcemia, familial, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "FBH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypocalciuric hypercalcemia, familial, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "familial hypocalciuric hypercalcemia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypocalciuric hypercalcemia, familial, type II; HHC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "familial benign hypercalcemia, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypocalciuric hypercalcemia type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "HHC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypercalcemia, familial benign, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "FHH type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007792", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007792", 
            "name": "hypercalcemia, familial benign type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060701", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060701", 
            "name": "FHH type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060701", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060701", 
            "name": "HHC2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060701", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060701", 
            "name": "familial hypocalciuric hypercalcemia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060701", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060701", 
            "name": "hypocalciuric hypercalcemia type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060701", 
        "description": "A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060701", 
        "name": "familial hypocalciuric hypercalcemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060701#disease-associations", 
            "id": "0060701", 
            "database": "Alliance of Genome Resources"
        }
    ]
}