{
    "disease_id": "DOID:0050477", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "Liddle syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "Liddle syndrome 1; LIDLS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "LIDLS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "Pseudoaldosteronism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "Liddle syndrome caused by mutation in SCNN1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020607", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020607", 
            "name": "SCNN1B Liddle syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050477", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050477", 
            "name": "Liddle's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050477", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050477", 
            "name": "Pseudoaldosteronism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050477", 
        "description": "A renal tubular transport disease that is characterized by hypertension and hypokalemia caused by dysregulation of epithelial sodium channels causing over expression of the channel.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050477", 
        "name": "Liddle syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050477#disease-associations", 
            "id": "0050477", 
            "database": "Alliance of Genome Resources"
        }
    ]
}