{
    "disease_id": "DOID:0080733",
    "recommended_name": {
        "id": "DOID:0080733",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080733",
        "name": "Ehlers-Danlos syndrome dermatosparaxis type",
        "description": "An Ehlers-Danlos syndrome that is characterized by severe skin fragility, sagging, redundant skin and that has_material_basis_in mutation in the gene encoding the procollagen protease ADAMTS2 on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "Ehlers-Danlos syndrome, dermatosparaxis type",
            "description": "A form of Ehlers-Danlos syndrome (EDS) characterized by extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and, sometimes, major complications due to visceral and vascular fragility."
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "dermatosparaxis",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "EDS VIIC",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "EDS 7C",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "dermatosparaxis EDS",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "dermatosparaxis Ehlers-Danlos syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "EDSDERMS",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "Ehlers-Danlos syndrome, dermatosparaxis type",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "Ehlers-Danlos syndrome, type VII, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "dEDS",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "Ehlers-Danlos syndrome type 7C (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "EDS7C",
            "description": ""
        },
        {
            "id": "MONDO:0009161",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009161",
            "name": "Ehlers-Danlos syndrome type 7C",
            "description": ""
        },
        {
            "id": "MIM:225410",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/225410",
            "name": "Ehlers-Danlos syndrome, dermatosparaxis type",
            "description": "Ehlers-Danlos syndrome, dermatosparaxis type"
        }
    ]
}