{
    "disease_id": "DOID:0060841", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "microphthalmia, isolated 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "MCOP8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "ALDH1A3 isolated microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "microphthalmia, isolated type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "isolated microphthalmia caused by mutation in ALDH1A3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "microphthalmia, isolated 8; MCOP8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014050", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014050", 
            "name": "isolated microphthalmia type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060841", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060841", 
            "name": "MCOP8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060841", 
        "description": "An isolated microphthalmia characterized by bilateral severe microphthalmia autosomal recessive inheritance of that has_material_basis_in homozygous mutation in the ALDH1A3 gene on chromosome 15q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060841", 
        "name": "isolated microphthalmia 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060841#disease-associations", 
            "id": "0060841", 
            "database": "Alliance of Genome Resources"
        }
    ]
}