{
    "disease_id": "DOID:0111532", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008150", 
            "name": "osteoglophonic dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008150", 
            "name": "OGD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008150", 
            "name": "Osteoglosphonic dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008150", 
            "name": "OSTEOGLOPHONIC dysplasia; OGD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008150", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008150", 
            "name": "Fairbank-Keats syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111532", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111532", 
            "name": "Fairbank-Keats syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111532", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111532", 
            "name": "OGD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111532", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111532", 
            "name": "osteoglophonic dwarfism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111532", 
        "description": "An osteochondrodysplasia characterized by rhizomelic dwarfism, craniosynostosis, prominent supraorbital ridge, depressed nasal bridge, nonossifying bone lesions, and multiple unerupted teeth that has_material_basis_in heterozygous missense mutation in FGFR1 on chromosome 8p11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111532", 
        "name": "osteoglophonic dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/166250", 
            "id": "166250", 
            "database": "MIM"
        }
    ]
}