{
    "disease_id": "DOID:0050630", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "FORSIUS-Eriksson type ocular albinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "AIED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "land Islands eye disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "ALAND ISLAND eye disease; AIED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "Forsius-Eriksson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010371", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010371", 
            "name": "Forsius Eriksson type ocular albinism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050630", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050630", 
            "name": "FORSIUS-ERIKSSON TYPE OCULAR ALBINISM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050630", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050630", 
            "name": "Forsius-Eriksson syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050630", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050630", 
        "name": "Aland Island eye disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050630#disease-associations", 
            "id": "0050630", 
            "database": "Alliance of Genome Resources"
        }
    ]
}