{
    "disease_id": "DOID:0110929",
    "recommended_name": {
        "id": "DOID:0110929",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110929",
        "name": "nemaline myopathy 9",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110929",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110929",
            "name": "NEM9",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "nemaline myopathy 9",
            "description": "Any nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene."
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "nemaline myopathy 9; NEM9",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "nemaline myopathy caused by mutation in KLHL41",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "nemaline myopathy type 9",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "nemaline myopathy 9",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "KLHL41 nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014326",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014326",
            "name": "NEM9",
            "description": ""
        },
        {
            "id": "MIM:615731",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615731",
            "name": "Nemaline myopathy 9",
            "description": "Nemaline myopathy 9"
        }
    ]
}