{
    "disease_id": "DOID:13269", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "Harderoporphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "Cpox deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "coproporphyria, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "CPRO deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "coproporphyria hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "HCP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "coproporphyrinogen oxidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "hereditary coproporphyria porphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "Cpx deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "porphyria hepatica II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "coproporphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "coproporphyria, hereditary; HCP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "porphyria hepatica coproporphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007369", 
            "name": "Cpo deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13269", 
            "name": "Coproporphyrinogen oxidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13269", 
            "name": "hereditary coproporphyria porphyria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13269", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:13269", 
        "name": "hereditary coproporphyria"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/121300", 
            "id": "121300", 
            "database": "MIM"
        }
    ]
}