{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "PITX2 iridogoniodysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis, type 2; IRID2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "irid 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "irid 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "anterior segment dysgenesis 4; ASGD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "IRID2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "IGDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "ASGD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iridogoniodysgenesis caused by mutation in PITX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007662", 
            "name": "iris hypoplasia with early-onset glaucoma, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080609", 
        "description": "An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the PITX2 gene on chromosome 4q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080609", 
        "name": "anterior segment dysgenesis 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/137600", 
            "id": "137600", 
            "database": "MIM"
        }
    ]
}