{
    "disease_id": "DOID:0060781",
    "recommended_name": {
        "id": "DOID:0060781",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060781",
        "name": "congenital secretory sodium diarrhea 3",
        "description": "A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0060781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060781",
            "name": "congenital secretory sodium diarrhea 3 syndromic",
            "description": ""
        },
        {
            "id": "DOID:0060781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060781",
            "name": "congenital secretory sodium diarrhoea 3",
            "description": ""
        },
        {
            "id": "DOID:0060781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060781",
            "name": "congenital secretory sodium diarrhoea 3 syndromic",
            "description": ""
        },
        {
            "id": "DOID:0060781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060781",
            "name": "congenital secretory sodium diarrhoea 3 with or without other congenital anomalies",
            "description": ""
        },
        {
            "id": "DOID:0060781",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060781",
            "name": "congenital secretory sodium diarrhea 3 with or without other congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "congenital secretory sodium diarrhea 3",
            "description": "Any secretory diarrhea in which the cause of the disease is a mutation in the SPINT2 gene."
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "SPINT2 secretory diarrhea",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "SPINT2 secretory diarrhoea",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "congenital secretory sodium diarrhea type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "congenital secretory sodium diarrhoea type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "secretory diarrhea caused by mutation in SPINT2",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "secretory diarrhoea caused by mutation in SPINT2",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "DIAR3",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "diarrhoea 3, secretory sodium, congenital, syndromic",
            "description": ""
        },
        {
            "id": "MONDO:0010036",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010036",
            "name": "diarrhoea 3, secretory sodium, congenital, with or without other congenital anomalies",
            "description": ""
        },
        {
            "id": "MIM:270420",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270420",
            "name": "Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies",
            "description": "Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060781"
    ],
    "unlinked_id_list": []
}