{
    "disease_id": "DOID:0110927", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "NEM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "nemaline myopathy 3, autosomal dominant or recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "myopathy, actin, congenital, with cores"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "ACTA1 nemaline myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "nemaline myopathy 3; NEM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "myopathy, actin, congenital, with Excess of thin myofilaments"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "nemaline myopathy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "nemaline myopathy caused by mutation in ACTA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008070", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008070", 
            "name": "nemaline myopathy 3, with intranuclear rods"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110927", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110927", 
            "name": "NEM3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110927", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110927", 
            "name": "nemaline myopathy 3, autosomal dominant or recessive"
        }, 
        {
            "url": "https://www.omim.org/entry/161800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:161800", 
            "name": "Myopathy, actin, congenital, with excess of thin myofilaments"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110927", 
        "description": "A nemaline myopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110927", 
        "name": "nemaline myopathy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/161800", 
            "id": "161800", 
            "database": "MIM"
        }
    ]
}