{
    "disease_id": "DOID:0110899", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "IL10RA inflammatory bowel disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "inflammatory bowel disease 28, autosomal recessive; IBD28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "inflammatory bowel disease 28, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "IBD28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "early onset autosomal recessive inflammatory bowel disease 28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "inflammatory bowel disease caused by mutation in IL10RA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "inflammatory bowel disease type 28"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013153", 
            "name": "inflammatory bowel disease, early-onset, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110899", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110899", 
            "name": "early onset autosomal recessive inflammatory bowel disease 28"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110899", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110899", 
            "name": "IBD28"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110899", 
        "description": "An inflammatory bowel disease characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the IL10RA gene on chromosome 11q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110899", 
        "name": "inflammatory bowel disease 28"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613148", 
            "id": "613148", 
            "database": "MIM"
        }
    ]
}