{
    "disease_id": "DOID:0110936", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "NEM5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "TNNT1 nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "Amish nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy 5, Amish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy caused by mutation in TNNT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy, Amish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "ANM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy 5; NEM5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011539", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011539", 
            "name": "nemaline myopathy, caused by mutation in the troponin t1 gene"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110936", 
            "name": "ANM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110936", 
            "name": "Amish nemaline myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110936", 
            "name": "NEM5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110936", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110936", 
            "name": "nemaline myopathy 5, Amish type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110936", 
        "description": "A nemaline myopathy that has_material_basis_in homozygous mutation in the TNNT1 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110936", 
        "name": "nemaline myopathy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110936#disease-associations", 
            "id": "0110936", 
            "database": "Alliance of Genome Resources"
        }
    ]
}