{
    "disease_id": "DOID:0110122",
    "recommended_name": {
        "id": "DOID:0110122",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110122",
        "name": "Axenfeld-Rieger syndrome type 3",
        "description": "An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25."
    },
    "synonyms": [
        {
            "id": "DOID:0110122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110122",
            "name": "RIEG3",
            "description": ""
        },
        {
            "id": "DOID:0110122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110122",
            "name": "Rieger syndrome type 3",
            "description": ""
        },
        {
            "id": "DOID:0110122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110122",
            "name": "Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss",
            "description": ""
        },
        {
            "id": "DOID:0110122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110122",
            "name": "anterior chamber cleavage syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110122",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110122",
            "name": "anterior segment mesenchymal dysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger syndrome type 3",
            "description": "Any Axenfeld-Rieger syndrome in which the cause of the disease is a mutation in the FOXC1 gene."
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger syndrome, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger syndrome, type 3; RIEG3",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "anterior chamber cleavage syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "anterior segment mesenchymal dysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Rieger syndrome, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger syndrome caused by mutation in FOXC1",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing loss",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "anterior chamber Cleavage syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Rieger anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "RIEG3",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Rieger syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "Axenfeld-Rieger anomaly with or without Cardiac defects and/or sensorineural hearing loss",
            "description": ""
        },
        {
            "id": "MONDO:0011233",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011233",
            "name": "FOXC1 Axenfeld-Rieger syndrome",
            "description": ""
        },
        {
            "id": "MIM:602482",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602482",
            "name": "Axenfeld-Rieger syndrome 3",
            "description": "Axenfeld-Rieger syndrome 3"
        }
    ]
}