{
    "disease_id": "DOID:0050477",
    "recommended_name": {
        "id": "DOID:0050477",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050477",
        "name": "Liddle syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0050477",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050477",
            "name": "Liddle's syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050477",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050477",
            "name": "Pseudoaldosteronism",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "Liddle syndrome 1",
            "description": "Any Liddle syndrome in which the cause of the disease is a mutation in the SCNN1B gene."
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "Liddle syndrome 1; LIDLS1",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "LIDLS1",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "Pseudoaldosteronism",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "Liddle syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "Liddle syndrome caused by mutation in SCNN1B",
            "description": ""
        },
        {
            "id": "MONDO:0020607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020607",
            "name": "SCNN1B Liddle syndrome",
            "description": ""
        },
        {
            "id": "MIM:177200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/177200",
            "name": "Liddle syndrome 1",
            "description": "Liddle syndrome 1"
        }
    ]
}