{
    "disease_id": "DOID:0110249", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "PITX3 early-onset non-syndromic cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "CTPP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "posterior polar cataract 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "cataract, posterior polar, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "CPP4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "Posterior polar cataract, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "cataract 11 with microphthalmia and neurodevelopmental abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "early-onset non-syndromic cataract caused by mutation in PITX3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "cataract 11, multiple types"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "CTRCT11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012527", 
            "name": "cataract 11, multiple types; CTRCT11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110249", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110249", 
            "name": "CTRCT11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110249", 
        "description": "A cataract that has_material_basis_in heterozygous mutation in the PITX3 gene on chromosome 10q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110249", 
        "name": "cataract 11 multiple types"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110249#disease-associations", 
            "id": "0110249", 
            "database": "Alliance of Genome Resources"
        }
    ]
}