{
    "disease_id": "DOID:0111532",
    "recommended_name": {
        "id": "DOID:0111532",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111532",
        "name": "osteoglophonic dysplasia",
        "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 the FGFR1 gene on chromosome 8p11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0111532",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111532",
            "name": "Fairbank-Keats syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111532",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111532",
            "name": "OGD",
            "description": ""
        },
        {
            "id": "DOID:0111532",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111532",
            "name": "osteoglophonic dwarfism",
            "description": ""
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "osteoglophonic dysplasia",
            "description": "A rare skeletal disorder characterized by dwarfism, severe craniofacial abnormalities and multiple unerupted teeth."
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "FGFR1-related osteoglophonic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "OGD",
            "description": ""
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "osteoglophonic dwarfism",
            "description": ""
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "osteoglophonic dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0008150",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008150",
            "name": "Fairbank-Keats syndrome",
            "description": ""
        },
        {
            "id": "MIM:166250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/166250",
            "name": "Osteoglophonic dysplasia",
            "description": "Osteoglophonic dysplasia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111532"
    ],
    "unlinked_id_list": []
}