{
    "disease_id": "DOID:0111375", 
    "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:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "FADS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "Pena-Shokeir syndrome type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "fetal akinesia sequence"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "foetal akinesia deformation sequence syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111375", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111375", 
            "name": "foetal akinesia sequence"
        }, 
        {
            "url": "https://www.omim.org/entry/208150", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:208150", 
            "name": "Fetal akinesia deformation sequence 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111375", 
        "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111375", 
        "name": "fetal akinesia deformation sequence syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/208150", 
            "id": "208150", 
            "database": "MIM"
        }
    ]
}