{
    "disease_id": "DOID:13269",
    "recommended_name": {
        "id": "DOID:13269",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13269",
        "name": "hereditary coproporphyria",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:13269",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13269",
            "name": "Coproporphyrinogen oxidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:13269",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13269",
            "name": "Hereditary coproporphyria",
            "description": ""
        },
        {
            "id": "DOID:13269",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13269",
            "name": "hereditary coproporphyria porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "hereditary coproporphyria",
            "description": "Hereditary coproporphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions."
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "Harderoporphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "Cpox deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "coproporphyria, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "CPRO deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "coproporphyria hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "HCP",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "coproporphyrinogen oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "hereditary coproporphyria porphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "Cpx deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "porphyria hepatica II",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "hereditary coproporphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "coproporphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "coproporphyria, hereditary; HCP",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "porphyria hepatica coproporphyria",
            "description": ""
        },
        {
            "id": "MONDO:0007369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007369",
            "name": "Cpo deficiency",
            "description": ""
        },
        {
            "id": "MIM:121300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/121300",
            "name": "Hereditary coproporphyria",
            "description": "Hereditary coproporphyria"
        }
    ]
}