{
    "disease_id": "DOID:0111377", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "fetal akinesia deformation sequence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "Pena-Shokeir syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "FADS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "Pena-Shokeir syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "arthrogryposis multiplex congenita with pulmonary hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "fetal akinesia sequence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008824", 
            "name": "fetal akinesia deformation sequence; FADS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111377", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111377", 
            "name": "FADS1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111377", 
        "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in MUSK on chromosome 9q31.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111377", 
        "name": "fetal akinesia deformation sequence syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111377#disease-associations", 
            "id": "0111377", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
