{
    "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": "hereditary acrokeratotic poikiloderma of Kindler-Weary",
            "description": ""
        },
        {
            "id": "MONDO:0008260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008260",
            "name": "poikiloderma, hereditary acrokeratotic",
            "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": "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": "KINDLER syndrome; KNDLRS",
            "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": "poikiloderma of Kindler",
            "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": "KS",
            "description": ""
        },
        {
            "id": "MIM:173650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/173650",
            "name": "Kindler syndrome",
            "description": "Kindler syndrome"
        }
    ]
}