{
    "disease_id": "DOID:0111785", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "frontometaphyseal dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "FMD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "FLNA frontometaphyseal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "FRONTOMETAPHYSEAL dysplasia 1; FMD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "frontometaphyseal dysplasia caused by mutation in FLNA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024550", 
            "name": "Fmd"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111785", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111785", 
            "name": "FMD"
        }, 
        {
            "url": "https://www.omim.org/entry/305620", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:305620", 
            "name": "Frontometaphyseal dysplasia 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111785", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111785", 
        "name": "frontometaphyseal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/305620", 
            "id": "305620", 
            "database": "MIM"
        }
    ]
}