{
    "disease_id": "DOID:0060472",
    "recommended_name": {
        "id": "DOID:0060472",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060472",
        "name": "Kindler syndrome",
        "description": "A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling."
    },
    "synonyms": [
        {
            "id": "DOID:0060472",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060472",
            "name": "poikiloderma of Kindler",
            "description": ""
        },
        {
            "id": "DOID:0060472",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060472",
            "name": "hereditary acrokeratotic poikiloderma of Kindler-Weary",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "Kindler syndrome",
            "description": "Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes."
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "KS",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "Kindler syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "poikiloderma of Kindler",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "KINDLER syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "KNDLRS",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "bullous acrokeratotic poikiloderma of Kindler and Weary",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "congenital bullous poikiloderma",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "poikiloderma, congenital, with bullae, Weary type",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "poikiloderma, hereditary acrokeratotic",
            "description": ""
        },
        {
            "id": "MIM:173650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/173650",
            "name": "Kindler syndrome",
            "description": "Kindler syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060472"
    ],
    "unlinked_id_list": []
}