{
    "disease_id": "DOID:0110931",
    "recommended_name": {
        "id": "DOID:0110931",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110931",
        "name": "nemaline myopathy 10",
        "description": "A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14."
    },
    "synonyms": [
        {
            "id": "DOID:0110931",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110931",
            "name": "NEM10",
            "description": ""
        },
        {
            "id": "DOID:0110931",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110931",
            "name": "congenital myopathy 10",
            "description": ""
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "nemaline myopathy 10",
            "description": "Any nemaline myopathy in which the cause of the disease is a mutation in the LMOD3 gene."
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "LMOD3 nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "NEM10",
            "description": ""
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "nemaline myopathy 10",
            "description": ""
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "nemaline myopathy caused by mutation in LMOD3",
            "description": ""
        },
        {
            "id": "MONDO:0014513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014513",
            "name": "nemaline myopathy type 10",
            "description": ""
        },
        {
            "id": "MIM:616165",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616165",
            "name": "Nemaline myopathy 10",
            "description": "Nemaline myopathy 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110931"
    ],
    "unlinked_id_list": []
}