{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "acroosteolysis dominant type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "HJCYS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "acroosteolysis with osteoporosis and changes in skull and mandible"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "Hajdu-Cheney syndrome; HJCYS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "serpentine fibula-polycystic kidneys syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "acrodentoosteodysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "Cheney syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "Arthrodentoosteodysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007057", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007057", 
            "name": "serpentine fibula-polycystic kidney syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "Cheney syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "HJCYS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "SFPKS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "arthrodentoosteodysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "acroosteolysis with osteoporosis and changes in skull and mandible"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2736", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2736", 
            "name": "serpentine fibula-polycystic kidney syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2736", 
        "description": "A bone disease characterized by short stature, coarse and dysmorphic facies, bowing of the long bones, and vertebral anomalies that has_material_basis_in heterozygous mutation in NOTCH2 on chromosome 1p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2736", 
        "name": "Hajdu-Cheney syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/102500", 
            "id": "102500", 
            "database": "MIM"
        }
    ]
}