{
    "disease_id": "DOID:0060375", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "OFD syndrome 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome type V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "Thurston syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "polydactyly postaxial with median cleft of upper lip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "oral facial digital syndrome type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "OFD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "oral-facial-digital syndrome type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome Thurston type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "oral facial digital syndrome 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "oral-facial-digital syndrome 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome, Thurston type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "polydactyly, postaxial, with Median cleft of upper lip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome V; OFD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "oral-Facial-digital syndrome, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "orofaciodigital syndrome type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008267", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008267", 
            "name": "Ofds 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060375", 
            "name": "polydactyly, postaxial, with median cleft of upper lip"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060375", 
            "name": "OFD5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060375", 
            "name": "orofaciodigital syndrome Thurston type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060375", 
        "description": "An orofaciodigital syndrome that is characterized by postaxial polydactyly and median cleft of the upper lip and has_material_basis_in homozygous mutation in the DDX59 gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060375", 
        "name": "orofaciodigital syndrome V"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060375#disease-associations", 
            "id": "0060375", 
            "database": "Alliance of Genome Resources"
        }
    ]
}