{
    "disease_id": "DOID:0080726", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers-Danlos syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers Danlos syndrome, mitis type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "EDS II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "EDSCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers Danlos syndrome, mild Classic type, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers-Danlos syndrome, type Ii, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers Danlos syndrome, mild Classic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers-Danlos syndrome, type Ii"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers-Danlos syndrome, classic type, 2; EDSCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "EDS II, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019568", 
            "name": "Ehlers Danlos syndrome, mitis type, formerly"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080726", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080726", 
        "name": "Ehlers-Danlos syndrome classic type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080726#disease-associations", 
            "id": "0080726", 
            "database": "Alliance of Genome Resources"
        }
    ]
}