{
    "disease_id": "DOID:0090067", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009232", 
            "name": "Fuhrmann-Rieger-de Sousa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009232", 
            "name": "fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009232", 
            "name": "fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009232", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009232", 
            "name": "bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090067", 
        "description": "A bone development disease that is characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the Wnt family member 7A (WNT7A) gene on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090067", 
        "name": "Fuhrmann syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090067#disease-associations", 
            "id": "0090067", 
            "database": "Alliance of Genome Resources"
        }
    ]
}