{
    "disease_id": "DOID:0060374", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "oral-facial-digital syndrome type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "Ofd syndrome with tibial defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "orofaciodigital syndrome type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "orofaciodigital syndrome with tibial dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "orofaciodigital syndrome 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "oral facial digital syndrome 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "orofaciodigital syndrome IV; OFD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "OFD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "OFD syndrome 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "Ofd syndrome, Baraitser-Burn type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "oral-Facial-digital syndrome, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "Baraitser-Burn syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "orofaciodigital syndrome type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "Ofds 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "oral facial digital syndrome type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009794", 
            "name": "Mohr-Majewski syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060374", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060374", 
            "name": "Baraitser-Burn syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060374", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060374", 
            "name": "OFD4"
        }, 
        {
            "url": "https://www.omim.org/entry/258860", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:258860", 
            "name": "Orofaciodigital syndrome 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060374", 
        "description": "An orofaciodigital syndrome that is characterized by dysmorphic facies, the development of harmartomas of the tongue, polydactyly and limb dysplasia, has_material_basis_in autosomal recessive inheritance of mutations in the TCTN3 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060374", 
        "name": "orofaciodigital syndrome IV"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/258860", 
            "id": "258860", 
            "database": "MIM"
        }
    ]
}