{
    "disease_id": "DOID:0080608",
    "recommended_name": {
        "id": "DOID:0080608",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080608",
        "name": "anterior segment dysgenesis 3",
        "description": "An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25."
    },
    "synonyms": [
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "anterior segment dysgenesis 3",
            "description": "An iridogoniodysgenesis that results from alterations in the forkhead transcription factor gene (FOXC1)"
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "anterior segment dysgenesis 3",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iris hypoplasia with glaucoma",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis anomaly, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "ASGD3",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "FOXC1 iridogoniodysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "IGDA syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "anterior segment dysgenesis 3; ASGD3",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "IGDS",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "glaucoma iridogoniodysplasia, familial",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "IRID1",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "IGDA",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis, type 1; IRID1",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "irid 1",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "glaucoma iridogoniodysgenesia",
            "description": ""
        },
        {
            "id": "MONDO:0024456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024456",
            "name": "iridogoniodysgenesis caused by mutation in FOXC1",
            "description": ""
        },
        {
            "id": "MIM:601631",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601631",
            "name": "Anterior segment dysgenesis 3",
            "description": "Anterior segment dysgenesis 3"
        }
    ]
}