{
    "disease_id": "DOID:3890", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria, Chester type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "pyrroloporphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "PBGD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "uroporphyrinogen synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "hydroxymethylbilane synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria, acute intermittent"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "HMBS deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria intermittent acute"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria, acute intermittent; AIP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria, acute intermittent, Nonerythroid variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "AIP - acute intermittent porphyria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "AIP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "UPS deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphobilinogen deaminase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008294", 
            "name": "porphyria, Swedish type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3890", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3890", 
            "name": "AIP - acute intermittent porphyria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3890", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3890", 
            "name": "Pyrroloporphyria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3890", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3890", 
            "name": "porphyria intermittent acute"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3890", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:3890", 
        "name": "acute intermittent porphyria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/3890#disease-associations", 
            "id": "3890", 
            "database": "Alliance of Genome Resources"
        }
    ]
}