{
    "disease_id": "DOID:0060776", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "diarrhea 5, with tufting enteropathy, congenital; DIAR5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "congenital tufting enteropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "diarrhea 5, with tufting enteropathy, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "secretory diarrhea caused by mutation in EPCAM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "enteropathy, congenital tufting"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "congenital familial intractable diarrhea with epithelial or epithelium abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "IED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "intestinal epithelial dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "congenital familial intractable diarrhea with enterocytes assembly abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "tufting enteropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "EPCAM secretory diarrhea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "DIAR5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "congenital enteropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013184", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013184", 
            "name": "intestinal epithelial cell dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "congenital familial intractable diarrhea with epithelial or epithelium abnormalities"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "DIAR5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "congenital diarrhoea 5 with tufting enteropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "congenital tufting enteropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "tufting enteropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060776", 
            "name": "congenital familial intractable diarrhoea with epithelial or epithelium abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060776", 
        "description": "A congenital diarrhea characterized by intractable diarrhea of infancy with villous atrophy, absence of inflammation, and intestinal epithelial cell dysplasia manifesting as focal epithelial tufts in the duodenum and jejunum that has_material_basis_in homozygous or compound heterozygous mutation in the EPCAM gene on chromosome 2p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060776", 
        "name": "congenital diarrhea 5 with tufting enteropathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060776#disease-associations", 
            "id": "0060776", 
            "database": "Alliance of Genome Resources"
        }
    ]
}