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