{
    "disease_id": "DOID:0111166",
    "recommended_name": {
        "id": "DOID:0111166",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111166",
        "name": "molybdenum cofactor deficiency type C",
        "description": "A molybdenum cofactor deficiency that has_material_basis_in homozygous mutation in the GPHN gene on chromosome 14q23."
    },
    "synonyms": [
        {
            "id": "DOID:0111166",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111166",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C",
            "description": ""
        },
        {
            "id": "DOID:0111166",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111166",
            "name": "MOCOD type C",
            "description": ""
        },
        {
            "id": "DOID:0111166",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111166",
            "name": "MOCODC",
            "description": ""
        },
        {
            "id": "DOID:0111166",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111166",
            "name": "molybdenum cofactor deficiency complementation group C",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type C",
            "description": "A molybdenum cofactor deficiency that has material basis in homozygous mutation in the GPHN gene on chromosome 14q23."
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "MOCOD type C",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "MOCODC",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "molybdenum cofactor deficiency C",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "molybdenum cofactor deficiency, complementation group type C",
            "description": ""
        },
        {
            "id": "MONDO:0014212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014212",
            "name": "molybdenum cofactor deficiency, complementation group C",
            "description": ""
        },
        {
            "id": "MIM:615501",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615501",
            "name": "Molybdenum cofactor deficiency C",
            "description": "Molybdenum cofactor deficiency C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111166"
    ],
    "unlinked_id_list": []
}