{
    "disease_id": "DOID:0060648", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "anterior segment dysgenesis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "ASMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "ASGD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "anterior segment mesenchymal dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "anterior segment dysgenesis 1; ASGD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "anterior segment ocular dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007138", 
            "name": "anterior segment mesenchymal dysgenesis; ASMD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060648", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060648", 
            "name": "anterior segment developmental anomaly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060648", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060648", 
            "name": "corneal opacification and other ocular anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060648", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060648", 
            "name": "sclerocornea with other ocular anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060648", 
        "description": "An eye disease that is characterized by iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface and is located_in the anterior segment of the eye.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060648", 
        "name": "anterior segment dysgenesis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060648#disease-associations", 
            "id": "0060648", 
            "database": "Alliance of Genome Resources"
        }
    ]
}