{
    "disease_id": "DOID:0080807", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "craniodiaphyseal dysplasia, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "craniodiaphyseal dysplasia, autosomal dominant; CDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "dominantly inherited craniodiaphyseal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "CDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "craniodiaphyseal dysplasia, dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021021", 
            "name": "Schaefer Stein Oshman syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/122860", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:122860", 
            "name": "Craniodiaphyseal dysplasia autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080807", 
        "description": "A craniodiaphyseal dysplasia that has_material_basis_in heterozygous mutation in the SOST gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080807", 
        "name": "autosomal dominant craniodiaphyseal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/122860", 
            "id": "122860", 
            "database": "MIM"
        }
    ]
}