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