{
    "disease_id": "DOID:0112149", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "terminal osseous dysplasia-pigmentary defects syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "terminal osseous dysplasia and pigmentary defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "terminal osseous dysplasia; TOD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "osseous dysplasia, digital, with Facial pigmentary defects and multiple frenula"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "Odpd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "Odpf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010279", 
            "name": "TOD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "ODPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "ODPF syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "TOD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "TODPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "terminal osseous dysplasia-pigmentary defects syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112149", 
            "name": "digital osseous dysplasia with facial pigmentary defects and multiple frenula"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112149", 
        "description": "A syndrome characterized by skeletal dysplasia of the limbs, pigmentary defects of the skin, and recurrent digital fibroma during infancy that has_material_basis_in heterozygous mutation in FLNA on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112149", 
        "name": "terminal osseous dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300244", 
            "id": "300244", 
            "database": "MIM"
        }
    ]
}