{
    "disease_id": "DOID:0080731",
    "recommended_name": {
        "id": "DOID:0080731",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080731",
        "name": "Ehlers-Danlos syndrome classic-like 1",
        "description": "An Ehlers-Danlos syndrome that is characterized by hyperextensible skin, hypermobile joints, and tissue fragility and that has_material_basis_in omozygous or heterozygous mutation in the tenascin-XB gene (TNXB) on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "Ehlers-Danlos syndrome due to tenascin-X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "EDS, classic-like type",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "Ehlers-Danlos syndrome due to tenascin-X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "Ehlers-Danlos syndrome, classic-like type",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "Ehlers-Danlos syndrome, classic-like, 1",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "EDS due to TNX deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "EDSCLL",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "Ehlers-Danlos-like syndrome due to tenascin-X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "TNX deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "clEDS",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "classical-like EDS",
            "description": ""
        },
        {
            "id": "MONDO:0011670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011670",
            "name": "classical-like Ehlers-Danlos syndrome",
            "description": ""
        },
        {
            "id": "MIM:606408",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606408",
            "name": "Ehlers-Danlos syndrome, classic-like, 1",
            "description": "Ehlers-Danlos syndrome, classic-like, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080731"
    ],
    "unlinked_id_list": []
}