{
    "disease_id": "DOID:0110932", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "nemaline myopathy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "TPM2 nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "nemaline myopathy 4; NEM4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "NEM4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "nemaline myopathy 4, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "nemaline myopathy caused by mutation in TPM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012240", 
            "name": "Cap myopathy 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110932", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110932", 
            "name": "NEM4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110932", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110932", 
            "name": "nemaline myopathy 4, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110932", 
        "description": "A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110932", 
        "name": "nemaline myopathy 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110932#disease-associations", 
            "id": "0110932", 
            "database": "Alliance of Genome Resources"
        }
    ]
}