{
    "disease_id": "DOID:0111533", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "osteogenesis imperfecta with unusual skeletal lesions"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "Levin syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "GDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "osteogenesis imperfecta Levin type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "GNATHODIAPHYSEAL dysplasia; GDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008151", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008151", 
            "name": "Gnathodiaphyseal sclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111533", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111533", 
            "name": "GDD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111533", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111533", 
            "name": "Levin syndrome 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111533", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111533", 
            "name": "gnathodiaphyseal sclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111533", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111533", 
            "name": "osteogenesis imperfecta, Levin type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111533", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111533", 
            "name": "osteogenesis imperfecta with unusual skeletal lesions"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111533", 
        "description": "An osteochondrodysplasia characterized by cementoosseous lesions of the jawbones, bone fragility, bowing/cortical thickening of tubular bones, and diaphyseal sclerosis of long bones that has_material_basis_in heterozygous mutation in ANO5 on chromosome11p14.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111533", 
        "name": "gnathodiaphyseal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111533#disease-associations", 
            "id": "0111533", 
            "database": "Alliance of Genome Resources"
        }
    ]
}