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