{
    "disease_id": "DOID:0080726",
    "recommended_name": {
        "id": "DOID:0080726",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080726",
        "name": "Ehlers-Danlos syndrome classic type 2",
        "description": "An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the collagen alpha-2(V) gene on chromosome 2q31 and that is characterized by the absence of widened atrophic scars."
    },
    "synonyms": [
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers-Danlos syndrome, classic type, 2",
            "description": "Any Ehlers-Danlos syndrome in which the cause of the disease is a mutation in the COL5A2 gene."
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "EDS II",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "EDSCL2",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers-Danlos syndrome, classic type, 2",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "EDS II, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers Danlos syndrome, mild Classic type",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers Danlos syndrome, mild Classic type, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers Danlos syndrome, mitis type",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers Danlos syndrome, mitis type, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers-Danlos syndrome, type Ii",
            "description": ""
        },
        {
            "id": "MONDO:0019568",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019568",
            "name": "Ehlers-Danlos syndrome, type Ii, formerly",
            "description": ""
        },
        {
            "id": "MIM:130010",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/130010",
            "name": "Ehlers-Danlos syndrome, classic type, 2",
            "description": "Ehlers-Danlos syndrome, classic type, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080726"
    ],
    "unlinked_id_list": []
}