{
    "disease_id": "DOID:0111783", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "otopalatodigital syndrome, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "Taybi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "oto-palato-digital syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "otopalatodigital syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "otopalatodigital syndrome, type I; OPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "OPD 1 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "otopalatodigital spectrum disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "OPD I syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "OPD syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "OPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "OPD syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010704", 
            "name": "frontootopalatodigital osteodysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "OPD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "OPD I syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "OPD syndrome 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "Taybi syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "oto-palato-digital syndrome type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111783", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111783", 
            "name": "otopalatodigital syndrome type I"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111783", 
        "description": "An otopalatodigital syndrome spectrum disorder characterized by cleft palate, mild skeletal anomalies including digital anomalies, and conductive deafness caused by ossicular anomalies that has_material_basis_in heterozygous or hemizygous mutation in exon 3, 4, or 5 of FLNA on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111783", 
        "name": "otopalatodigital syndrome type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111783#disease-associations", 
            "id": "0111783", 
            "database": "Alliance of Genome Resources"
        }
    ]
}