{
    "disease_id": "DOID:0060342", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011359", 
            "name": "acromelic frontonasal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011359", 
            "name": "AFND"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011359", 
            "name": "acromelic frontonasal dysostosis; AFND"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011359", 
            "name": "frontonasal dysplasia acromelic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011359", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011359", 
            "name": "Toriello syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060342", 
        "description": "A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060342", 
        "name": "acromelic frontonasal dysostosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060342#disease-associations", 
            "id": "0060342", 
            "database": "Alliance of Genome Resources"
        }
    ]
}