{
    "disease_id": "DOID:0070356",
    "recommended_name": {
        "id": "DOID:0070356",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070356",
        "name": "visual impairment and progressive phthisis bulbi",
        "description": "An eye disease that is characterized by poor vision at birth, with development of bilateral phthisis by adulthood and that has_material_basis_in homozygous mutation in the MARK3 gene on chromosome 14q3."
    },
    "synonyms": [
        {
            "id": "MONDO:0032655",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032655",
            "name": "visual impairment and progressive phthisis bulbi",
            "description": ""
        },
        {
            "id": "MONDO:0032655",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032655",
            "name": "VIPB",
            "description": ""
        },
        {
            "id": "MONDO:0032655",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032655",
            "name": "VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI",
            "description": ""
        },
        {
            "id": "MIM:618283",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618283",
            "name": "Visual impairment and progressive phthisis bulbi",
            "description": "Visual impairment and progressive phthisis bulbi"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070356"
    ],
    "unlinked_id_list": []
}