{
    "disease_id": "DOID:0060775", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "MVD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "DIAR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "microvillous inclusion disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "diarrhea 2, with microvillus atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "Davidson's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "congenital microvillus atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "familial enteropathy, microvillus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "Davidson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "congenital familial protracted diarrhea with enterocyte Brush-border abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "MYO5B secretory diarrhea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "microvillus atrophy, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "diarrhea 2, with microvillus atrophy; DIAR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "diarrhea 2 with microvillus atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "MVID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "intractable diarrhea of infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "congenital microvillous atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "secretory diarrhea caused by mutation in MYO5B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009635", 
            "name": "congenital familial protracted diarrhea"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "congenital familial protracted diarrhea with enterocyte brush-border abnormalities"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "Davidson disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "MVD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "congenital microvillus atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "diarrhea 2 with microvillus atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060775", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060775", 
            "name": "intractable diarrhea of infancy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060775", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060775", 
        "name": "microvillus inclusion disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060775#disease-associations", 
            "id": "0060775", 
            "database": "Alliance of Genome Resources"
        }
    ]
}