{
    "disease_id": "DOID:0060778",
    "recommended_name": {
        "id": "DOID:0060778",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060778",
        "name": "congenital diarrhea 7 with exudative enteropathy",
        "description": "A congenital diarrhea characterized by early-onset nonbloody watery diarrhea and unresponsiveness to soy-based or elemental formulas that has_material_basis_in homozygous or compound heterozygous mutation in the DGAT1 gene on chromosome 8q24."
    },
    "synonyms": [
        {
            "id": "DOID:0060778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060778",
            "name": "congenital chronic diarrhoea with protein-losing enteropathy",
            "description": ""
        },
        {
            "id": "DOID:0060778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060778",
            "name": "congenital diarrhoea 7 with exudative enteropathy",
            "description": ""
        },
        {
            "id": "DOID:0060778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060778",
            "name": "congenital chronic diarrhea with exudative enteropathy",
            "description": ""
        },
        {
            "id": "DOID:0060778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060778",
            "name": "congenital chronic diarrhea with protein-losing enteropathy",
            "description": ""
        },
        {
            "id": "DOID:0060778",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060778",
            "name": "congenital chronic diarrhoea with exudative enteropathy",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "congenital diarrhea 7 with exudative enteropathy",
            "description": "Congenital chronic diarrhea with protein-losing enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema."
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "DGAT1 congenital diarrhea",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "DGAT1 congenital diarrhoea",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "congenital chronic diarrhea with exudative enteropathy",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "congenital chronic diarrhea with protein-losing enteropathy",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "congenital diarrhea caused by mutation in DGAT1",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "congenital diarrhoea caused by mutation in DGAT1",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhea 7, protein-losing enteropathy type",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhea type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhoea 7, protein-losing enteropathy type",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhoea type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "DIAR7",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhea 7",
            "description": ""
        },
        {
            "id": "MONDO:0014375",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014375",
            "name": "diarrhoea 7",
            "description": ""
        },
        {
            "id": "MIM:615863",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615863",
            "name": "Diarrhea 7, protein-losing enteropathy type",
            "description": "Diarrhea 7, protein-losing enteropathy type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060778"
    ],
    "unlinked_id_list": []
}