{
    "disease_id": "DOID:0111785",
    "recommended_name": {
        "id": "DOID:0111785",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111785",
        "name": "frontometaphyseal dysplasia",
        "description": "An otopalatodigital syndrome spectrum disorder characterized by abnormal ossification and skeletal patterning of the axial and appendicular skeleton, facial dysmorphism, urogenital anomalies, and hearing loss."
    },
    "synonyms": [
        {
            "id": "DOID:0111785",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111785",
            "name": "FMD",
            "description": ""
        },
        {
            "id": "MONDO:0024550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024550",
            "name": "frontometaphyseal dysplasia 1",
            "description": "Any frontometaphyseal dysplasia in which the cause of the disease is a mutation in the FLNA gene."
        },
        {
            "id": "MONDO:0024550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024550",
            "name": "FLNA frontometaphyseal dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0024550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024550",
            "name": "frontometaphyseal dysplasia 1, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0024550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024550",
            "name": "frontometaphyseal dysplasia caused by mutation in FLNA",
            "description": ""
        },
        {
            "id": "MONDO:0024550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024550",
            "name": "FMD1",
            "description": ""
        },
        {
            "id": "MIM:305620",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/305620",
            "name": "Frontometaphyseal dysplasia 1",
            "description": "Frontometaphyseal dysplasia 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0111786",
            "label": "frontometaphyseal dysplasia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111787",
            "label": "frontometaphyseal dysplasia 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0111787",
        "DOID:0111786",
        "DOID:0111785"
    ],
    "unlinked_id_list": []
}