{
    "disease_id": "DOID:13271",
    "recommended_name": {
        "id": "DOID:13271",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13271",
        "name": "cutaneous porphyria",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:13271",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13271",
            "name": "Erythropoietic porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "cutaneous porphyria",
            "description": "Congenital erythropoietic porphyria, or Gnther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis."
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "uroporphyrinogen 3 synthase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "Gunther disease",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "congenital porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "Uros deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "CEP",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "porphyria, congenital erythropoietic",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "congenital erythropoietic porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "erythropoietic porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "uroporphyrinogen III synthase, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "Gnther disease",
            "description": ""
        },
        {
            "id": "MONDO:0009902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009902",
            "name": "Cep",
            "description": ""
        },
        {
            "id": "MIM:263700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/263700",
            "name": "Congenital erythropoietic porphyria",
            "description": "Congenital erythropoietic porphyria"
        }
    ]
}