{
    "disease_id": "DOID:0111765", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "cardiac valvular dysplasia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "valvular heart disease, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "CARDIAC valvular dysplasia, X-linked; CVD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "myxomatous valvular dystrophy, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "CVD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010753", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010753", 
            "name": "XMVD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "CVD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "XMVD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "FLNA-related X-linked myxomatous valvular dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "Dystrophie valvulaire associee a FLNA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "EDS 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "Ehlers-Danlos syndrome, type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "FLNA-related valvular dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111765", 
            "name": "Filamin A-related X-linked myxomatous valvular dysplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111765", 
        "description": "A heart valve disease characterized by multivalvular dysplasia and regurgitation with more severe phenotypes in hemizygous males compared to heterozygous females that has_material_basis_in mutation in FLNA on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111765", 
        "name": "X-linked cardiac valvular dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111765#disease-associations", 
            "id": "0111765", 
            "database": "Alliance of Genome Resources"
        }
    ]
}