{
    "disease_id": "DOID:0110933",
    "recommended_name": {
        "id": "DOID:0110933",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110933",
        "name": "nemaline myopathy 11",
        "description": "A nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110933",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110933",
            "name": "NEM11",
            "description": ""
        },
        {
            "id": "DOID:0110933",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110933",
            "name": "nemaline myopathy 11, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "nemaline myopathy 11",
            "description": "Any nemaline myopathy in which the cause of the disease is a mutation in the MYPN gene."
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "nemaline myopathy caused by mutation in MYPN",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "nemaline myopathy 11, autosomal recessive; NEM11",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "nemaline myopathy type 11",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "nemaline myopathy 11, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "MYPN nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0015023",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015023",
            "name": "NEM11",
            "description": ""
        },
        {
            "id": "MIM:617336",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617336",
            "name": "Nemaline myopathy 11",
            "description": "Nemaline myopathy 11"
        }
    ]
}