{
    "disease_id": "DOID:0110267", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "cataract type 44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "cataract 44; CTRCT44"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "early-onset non-syndromic cataract caused by mutation in LSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "total early-onset cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "LSS early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014673", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014673", 
            "name": "CTRCT44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110267", 
            "name": "CTRCT44"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110267", 
            "name": "total early-onset cataract"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110267", 
        "description": "A cataract that has_material_basis_in homozygous mutation in the LSS gene on chromosome 21q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110267", 
        "name": "cataract 44"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110267#disease-associations", 
            "id": "0110267", 
            "database": "Alliance of Genome Resources"
        }
    ]
}