{
    "disease_id": "DOID:2106",
    "recommended_name": {
        "id": "DOID:2106",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2106",
        "name": "myotonia congenita",
        "description": "A muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres."
    },
    "synonyms": [
        {
            "id": "DOID:2106",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2106",
            "name": "Congenital myotonia, autosomal dominant form",
            "description": ""
        },
        {
            "id": "DOID:2106",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2106",
            "name": "Thomsen disease",
            "description": ""
        },
        {
            "id": "DOID:2106",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2106",
            "name": "Thomsen's disease",
            "description": ""
        },
        {
            "id": "MONDO:0008055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008055",
            "name": "myotonia congenita, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008055",
            "name": "myotonia Levior",
            "description": ""
        },
        {
            "id": "MONDO:0008055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008055",
            "name": "Thomsen disease",
            "description": ""
        },
        {
            "id": "MONDO:0008055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008055",
            "name": "myotonia congenita, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0009715",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009715",
            "name": "myotonia congenita, autosomal recessive",
            "description": "Autosomal recessive form of myotonia congenita."
        },
        {
            "id": "MONDO:0009715",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009715",
            "name": "autosomal recessive myotonia congenita",
            "description": ""
        },
        {
            "id": "MONDO:0009715",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009715",
            "name": "myotonia, generalized",
            "description": ""
        },
        {
            "id": "MONDO:0009715",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009715",
            "name": "Becker disease",
            "description": ""
        },
        {
            "id": "MONDO:0009715",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009715",
            "name": "myotonia congenita, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:160800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/160800",
            "name": "Myotonia congenita, autosomal dominant",
            "description": "Myotonia congenita, autosomal dominant"
        },
        {
            "id": "MIM:255700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/255700",
            "name": "Myotonia congenita, autosomal recessive",
            "description": "Myotonia congenita, autosomal recessive"
        }
    ]
}