{
    "disease_id": "DOID:0080033", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "craniometaphyseal dysplasia, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "CMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "CMDJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "craniometaphyseal dysplasia, Jackson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "CMDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "craniometaphyseal dysplasia Jackson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007397", 
            "name": "craniometaphyseal dysplasia, autosomal dominant; CMDD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080033", 
        "description": "An osteosclerosis that is characterized by hyperostosis and sclerosis of the craniofacial bones associated with abnormal modeling of the metaphyses.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080033", 
        "name": "craniometaphyseal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080033#disease-associations", 
            "id": "0080033", 
            "database": "Alliance of Genome Resources"
        }
    ]
}