{
    "disease_id": "DOID:0060775",
    "recommended_name": {
        "id": "DOID:0060775",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060775",
        "name": "microvillus inclusion disease",
        "description": "A congenital diarrhea characterized by onset of intractable life-threatening watery diarrhea during infancy, lack of microvilli on the surface of enterocytes and occurrence of intracellular vacuolar structures containing microvilli that has_material_basis_in homozygous or compound heterozygous mutation in the MYO5B gene on chromosome 18q21."
    },
    "synonyms": [
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "congenital familial protracted diarrhea with enterocyte brush-border abnormalities",
            "description": ""
        },
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "Davidson disease",
            "description": ""
        },
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "MVD",
            "description": ""
        },
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "congenital microvillus atrophy",
            "description": ""
        },
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "diarrhea 2 with microvillus atrophy",
            "description": ""
        },
        {
            "id": "DOID:0060775",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060775",
            "name": "intractable diarrhea of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "microvillus inclusion disease",
            "description": "Microvillus inclusion disease (MVID) is a very rare, severe, malabsorbative syndrome characterized clinically by protracted or intractable neonatal secretory diarrhea and histologically by inclusion bodies on the intestinal epithelium."
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "Davidson disease",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "MVID",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "MYO5B secretory diarrhea",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "MYO5B secretory diarrhoea",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital familial protracted diarrhea with enterocyte brush-border abnormalities",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital familial protracted diarrhoea with enterocyte brush-border abnormalities",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital microvillous atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital microvillus atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "diarrhoea 2 with microvillus atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "microvillous inclusion disease",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "microvillus inclusion disease",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "secretory diarrhea caused by mutation in MYO5B",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "secretory diarrhoea caused by mutation in MYO5B",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "DIAR2",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "Davidson's disease",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital familial protracted diarrhea",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital familial protracted diarrhoea",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "congenital familial protracted diarrhoea with enterocyte Brush-border abnormalities",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "diarrhea 2, with microvillus atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "diarrhoea 2, with microvillus atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "familial enteropathy, microvillus",
            "description": ""
        },
        {
            "id": "MONDO:0009635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009635",
            "name": "intractable diarrhoea of infancy",
            "description": ""
        },
        {
            "id": "MIM:251850",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/251850",
            "name": "Diarrhea 2, with microvillus atrophy, with or without cholestasis",
            "description": "Diarrhea 2, with microvillus atrophy, with or without cholestasis"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060775"
    ],
    "unlinked_id_list": []
}