{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "OCT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "OTC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "deficiency of citrulline phosphorylase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "ornithine transcarbamylase deficiency, hyperammonemia due to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "valproate sensitivity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "ornithine transcarbamylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "ornithine carbamoyltransferase deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010703", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010703", 
            "name": "OTCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9271", 
            "name": "deficiency of citrulline phosphorylase"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9271", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9271", 
            "name": "ornithine transcarbamylase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9271", 
        "description": "An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9271", 
        "name": "ornithine carbamoyltransferase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/311250", 
            "id": "311250", 
            "database": "MIM"
        }
    ]
}