{
    "disease_id": "DOID:0080670",
    "recommended_name": {
        "id": "DOID:0080670",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080670",
        "name": "Meesmann corneal dystrophy 1",
        "description": "A Messmann corneal dystrophy that is characterized by the presence of multitudinous microcysts within the anterior epithelium and that has_material_basis_in heterozygous mutation in the KRT12 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0020791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020791",
            "name": "corneal dystrophy, Meesmann, 1",
            "description": ""
        },
        {
            "id": "MONDO:0020791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020791",
            "name": "MECD1",
            "description": ""
        },
        {
            "id": "MIM:122100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/122100",
            "name": "Corneal dystrophy, Meesmann 1",
            "description": "Corneal dystrophy, Meesmann 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080670"
    ],
    "unlinked_id_list": []
}