{
    "disease_id": "DOID:0111679", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "formiminoglutamic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "formiminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "formiminotransferase deficiency syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "Formiminoglutamicaciduria (FIGLU-Uria)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "formiminotransferase cyclodeaminase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "Figlu-Uria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "Arakawa syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "FTCD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009240", 
            "name": "formiminoglutamic acidemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "Arakawa syndrome 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "FIGLUria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "FTCD deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "formiminoglutamic acidemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "formiminoglutamic aciduria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "formiminotransferase cyclodeaminase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111679", 
            "name": "formiminotransferase deficiency syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111679", 
        "description": "A vitamin metabolic disorder characterized by elevated formiminoglutamate in urine and plasma and variable intellectual, developmental, and hematological phenotypes that has_material_basis_in homozygous or compound heterozygous mutation in FTCD on chromosome 21q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111679", 
        "name": "glutamate formiminotransferase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/229100", 
            "id": "229100", 
            "database": "MIM"
        }
    ]
}