{
    "disease_id": "DOID:0110936",
    "recommended_name": {
        "id": "DOID:0110936",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110936",
        "name": "nemaline myopathy 5A",
        "description": "A nemaline myopathy that has_material_basis_in autosomal recessive inheritance of a homozygous mutation in the TNNT1 gene on chromosome 19q13, with infantile onset."
    },
    "synonyms": [
        {
            "id": "DOID:0110936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110936",
            "name": "ANM",
            "description": ""
        },
        {
            "id": "DOID:0110936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110936",
            "name": "Amish nemaline myopathy",
            "description": ""
        },
        {
            "id": "DOID:0110936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110936",
            "name": "NEM5",
            "description": ""
        },
        {
            "id": "DOID:0110936",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110936",
            "name": "nemaline myopathy 5, Amish type",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy 5",
            "description": "Amish nemaline myopathy is a type of nemaline myopathy (NM) only observed in several families of the Amish community."
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "ANM",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "Amish nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "NEM5",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "TNNT1 nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy 5",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy 5, Amish type",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy caused by mutation in TNNT1",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy, Amish type",
            "description": ""
        },
        {
            "id": "MONDO:0011539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011539",
            "name": "nemaline myopathy, caused by mutation in the troponin t1 gene",
            "description": ""
        },
        {
            "id": "MIM:605355",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605355",
            "name": "Nemaline myopathy 5A, autosomal recessive, severe infantile",
            "description": "Nemaline myopathy 5A, autosomal recessive, severe infantile"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110936"
    ],
    "unlinked_id_list": []
}