{
    "disease_id": "DOID:0050720",
    "recommended_name": {
        "id": "DOID:0050720",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050720",
        "name": "ornithine translocase deficiency",
        "description": "An amino acid metabolic disorder that has_material_basis_in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood."
    },
    "synonyms": [
        {
            "id": "DOID:0050720",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050720",
            "name": "Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050720",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050720",
            "name": "HHH syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "ornithine translocase deficiency",
            "description": "A rare, genetic disorder of urea cycle metabolism characterized by either a neonatal-onset with manifestations of lethargy, poor feeding, vomiting and tachypnea or, more commonly, presentations in infancy, childhood or adulthood with chronic neurocognitive deficits, acute encephalopathy and/or coagulation defects or other chronic liver dysfunction."
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "HHH syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "ORNT1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "hyperornithinemia-hyperammonemia-homocitrullinemia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "ornithine carrier deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "ornithine translocase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "triple H syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "HHH",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "HHHS",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "Hhh syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "hyperornithinemia-hyperammonemia-homocitrullinuria syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009393",
            "name": "ornithine translocase deficiency syndrome",
            "description": ""
        },
        {
            "id": "MIM:238970",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/238970",
            "name": "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome",
            "description": "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050720"
    ],
    "unlinked_id_list": []
}