{
    "disease_id": "DOID:0080612", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "sclerocornea with Other ocular anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "CCMCO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "COPOA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "corneal opacification and other ocular anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "congenital cataract microcornea with corneal opacity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "anterior segment dysgenesis 7; ASGD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "corneal opacification with Other ocular anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "ASGD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "PXDN anterior segment dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "corneal opacification with other ocular anomalies; COPOA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010015", 
            "name": "anterior segment dysgenesis caused by mutation in PXDN"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080612", 
        "description": "An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080612", 
        "name": "anterior segment dysgenesis 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080612#disease-associations", 
            "id": "0080612", 
            "database": "Alliance of Genome Resources"
        }
    ]
}