{
    "disease_id": "DOID:0060849", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "OPPG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "osteoporosis pseudoglioma syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "Ops"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "ocular form of osteogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "pseudoglioma with bone fragility"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "osteogenesis imperfecta ocular form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "osteoporosis-pseudoglioma syndrome; OPPG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009820", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009820", 
            "name": "osteogenesis imperfecta, ocular form"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060849", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060849", 
            "name": "OPPG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060849", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060849", 
            "name": "ocular form of osteogenesis imperfecta"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060849", 
        "description": "A syndrome characterized by congenital or infancy-onset blindness, very low bone mass, decreased trabecular bone volume, severe juvenile-onset osteoporosis and spontaneous fractures, pseudoglioma, microphthalmia  that has_material_basis_in homozygous or compound heterozygous mutation in the LRP5 gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060849", 
        "name": "osteoporosis-pseudoglioma syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060849#disease-associations", 
            "id": "0060849", 
            "database": "Alliance of Genome Resources"
        }
    ]
}