{
    "disease_id": "DOID:0050884", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014221", 
            "name": "triose phosphate-isomerase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014221", 
            "name": "TPI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014221", 
            "name": "TPID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014221", 
            "name": "triosephosphate isomerase deficiency; TPID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050884", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050884", 
            "name": "Triose phosphate-isomerase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050884", 
        "description": "A glucose metabolism disorder that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections and severe neurological dysfunction, and has_material_basis_in the triosephosphate isomerase enzyme (TPI1) gene inherited as an autosomal recessive trait.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050884", 
        "name": "triosephosphate isomerase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615512", 
            "id": "615512", 
            "database": "MIM"
        }
    ]
}