{
    "disease_id": "DOID:14671", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "multiple gastrointestinal atresias"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "gastrointestinal defects and immunodeficiency syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "combined immunodeficiency-enteropathy spectrum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "Cid-MIA/early-onset IBD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "GIDID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "intestinal atresia multiple"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "gastrointestinal defects and immunodeficiency syndrome; GIDID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "intestinal atresia, multiple"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009465", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009465", 
            "name": "familial intestinal polyatresia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14671", 
            "name": "gastrointestinal defects and immunodeficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14671", 
            "name": "GIDID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14671", 
            "name": "MEDDRA:10028210"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14671", 
            "name": "Multiple gastrointestinal atresias"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14671", 
            "name": "familial intestinal polyatresia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14671", 
        "description": "An intestinal disease characterized by the presence of numerous atresic segments in the small and large intestines that has_material_basis_in homozygous or compound heterozygous mutation in TTC7A on chromosome 2p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14671", 
        "name": "multiple intestinal atresia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14671#disease-associations", 
            "id": "14671", 
            "database": "Alliance of Genome Resources"
        }
    ]
}