{
    "disease_id": "DOID:0110933", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "nemaline myopathy caused by mutation in MYPN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "nemaline myopathy 11, autosomal recessive; NEM11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "nemaline myopathy type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "nemaline myopathy 11, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "MYPN nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0015023", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0015023", 
            "name": "NEM11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110933", 
            "name": "NEM11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110933", 
            "name": "nemaline myopathy 11, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110933", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110933", 
        "name": "nemaline myopathy 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110933#disease-associations", 
            "id": "0110933", 
            "database": "Alliance of Genome Resources"
        }
    ]
}