{
    "disease_id": "DOID:0110929", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014326", 
            "name": "nemaline myopathy 9; NEM9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014326", 
            "name": "nemaline myopathy caused by mutation in KLHL41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014326", 
            "name": "nemaline myopathy type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014326", 
            "name": "KLHL41 nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014326", 
            "name": "NEM9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110929", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110929", 
            "name": "NEM9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110929", 
        "description": "A nemaline myopathy characterized by onset in early infancy of muscle weakness with variable severity that has_material_basis_in homozygous or compound heterozygous mutation in the KLHL41 gene on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110929", 
        "name": "nemaline myopathy 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615731", 
            "id": "615731", 
            "database": "MIM"
        }
    ]
}