{
    "disease_id": "DOID:0111438", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012543", 
            "name": "OPA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012543", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012543", 
            "name": "optic atrophy 5; OPA5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111438", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111438", 
            "name": "OPA5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111438", 
        "description": "An optic atrophy characterized by degeneration of retinal ganglion cells resulting in slowly progressive visual loss with variable onset from the first to third decades that has_material_basis_in heterozygous of mutation in DNM1L on chromosome 12p11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111438", 
        "name": "optic atrophy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111438#disease-associations", 
            "id": "0111438", 
            "database": "Alliance of Genome Resources"
        }
    ]
}