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