{
    "disease_id": "DOID:0050630",
    "recommended_name": {
        "id": "DOID:0050630",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050630",
        "name": "Aland Island eye disease",
        "description": "An eye disease characterized by fundus hypopigmentation, decreased visual acuity, nystagmus, astigmatism, myopia and defective darkness adaptation and has_material_basis_in mutation in the CACNA1F gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050630",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050630",
            "name": "FORSIUS-ERIKSSON TYPE OCULAR ALBINISM",
            "description": ""
        },
        {
            "id": "DOID:0050630",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050630",
            "name": "Forsius-Eriksson syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "Aland island eye disease",
            "description": "An X-linked recessive retinal disease characterized by fundus hypopigmentation, decrased visual acuity, nystagmus, astigmatism, progressive axial myopia, defective dark adaptation and protanopia."
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "AIED",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "Aland island eye disease",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "FORSIUS-Eriksson type ocular albinism",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "Forsius-Eriksson syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "Forsius-Eriksson type ocular albinism",
            "description": ""
        },
        {
            "id": "MONDO:0010371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010371",
            "name": "Forsius Eriksson type ocular albinism",
            "description": ""
        },
        {
            "id": "MIM:300600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300600",
            "name": "Aaland island eye disease",
            "description": "Aaland island eye disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050630"
    ],
    "unlinked_id_list": []
}