{
    "disease_id": "DOID:0060781", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "congenital secretory sodium diarrhea 3 with or without other congenital anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "SPINT2 secretory diarrhea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "diarrhea 3, secretory sodium, congenital, syndromic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "congenital secretory sodium diarrhea 3 syndromic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies; DIAR3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "congenital secretory sodium diarrhea type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "secretory diarrhea caused by mutation in SPINT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "sodium diarrhea, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010036", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010036", 
            "name": "DIAR3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060781", 
            "name": "congenital secretory sodium diarrhea 3 syndromic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060781", 
            "name": "congenital secretory sodium diarrhoea 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060781", 
            "name": "congenital secretory sodium diarrhoea 3 syndromic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060781", 
            "name": "congenital secretory sodium diarrhoea 3 with or without other congenital anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060781", 
            "name": "congenital secretory sodium diarrhea 3 with or without other congenital anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060781", 
        "description": "A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060781", 
        "name": "congenital secretory sodium diarrhea 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060781#disease-associations", 
            "id": "0060781", 
            "database": "Alliance of Genome Resources"
        }
    ]
}