{
    "disease_id": "DOID:0090018", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "Hibernian fever, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "TNF receptor-associated periodic fever syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "FPF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "FHF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "periodic FEVER, familial, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "tumor necrosis factor receptor 1 associated periodic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "TNF receptor-associated periodic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "TNF receptor 1-associated periodic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "tumor necrosis factor receptor-associated periodic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "TRAPS syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "tumor necrosis factor receptor 1-associated periodic syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "TRAPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007727", 
            "name": "familial Hibernian fever"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090018", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090018", 
            "name": "TNF receptor 1-associated periodic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090018", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090018", 
            "name": "tumor necrosis factor receptor 1 associated periodic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090018", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090018", 
            "name": "familial Hibernian fever"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090018", 
        "description": "A primary immunodeficiency disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090018", 
        "name": "autosomal dominant familial periodic fever"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090018#disease-associations", 
            "id": "0090018", 
            "database": "Alliance of Genome Resources"
        }
    ]
}