{
    "disease_id": "DOID:0111816", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "Zygodactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "Sd1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "syndactyly, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "chromosome 2q35 DUPLICATION syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "craniosynostosis, Philadelphia type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008512", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008512", 
            "name": "SDTY1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111816", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111816", 
            "name": "chromosome 2q35 duplication syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111816", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111816", 
            "name": "syndactyly, type 1, with or without craniosynostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111816", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111816", 
            "name": "SDTY1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111816", 
        "description": "A syndactyly characterized by complete or partial webbing between the third and fourth fingers and/or the second and third toes that has_material_basis_in heterozygous duplication of a region of chromosome 2q34-q36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111816", 
        "name": "syndactyly type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111816#disease-associations", 
            "id": "0111816", 
            "database": "Alliance of Genome Resources"
        }
    ]
}