{
    "disease_id": "DOID:14756", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "autosomal dominant Ehlers-Danlos syndrome, vascular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "EDSVASC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, Ecchymotic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, vascular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, vascular type; EDSVASC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, type IV, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, vascular type, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, sack-Barabas type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "EDS 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "autosomal dominant type IV Ehlers-Danlos syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007524", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007524", 
            "name": "Ehlers-Danlos syndrome, arterial type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14756", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14756", 
            "name": "autosomal dominant type IV Ehlers-Danlos syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/130050", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:130050", 
            "name": "Ehlers-Danlos syndrome, vascular type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14756", 
        "description": "An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the COL3A1 gene on chromosome 2q32 and that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14756", 
        "name": "vascular type Ehlers-Danlos syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/130050", 
            "id": "130050", 
            "database": "MIM"
        }
    ]
}