{
    "disease_id": "DOID:0080512", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "Meier-GORLIN syndrome 1; MGORS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "ORC1 Meier-Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "Meier-Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "microtia, absent patellae, micrognathia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "Ear, patella, short stature syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "Meier-Gorlin syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "MGORS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009143", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009143", 
            "name": "Meier-Gorlin syndrome caused by mutation in ORC1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080512", 
        "description": "A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080512", 
        "name": "Meier-Gorlin syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080512#disease-associations", 
            "id": "0080512", 
            "database": "Alliance of Genome Resources"
        }
    ]
}