{
    "disease_id": "DOID:0111164",
    "recommended_name": {
        "id": "DOID:0111164",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111164",
        "name": "molybdenum cofactor deficiency type A",
        "description": "A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "DOID:0111164",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111164",
            "name": "MOCOD type A",
            "description": ""
        },
        {
            "id": "DOID:0111164",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111164",
            "name": "MOCODA",
            "description": ""
        },
        {
            "id": "DOID:0111164",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111164",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A",
            "description": ""
        },
        {
            "id": "DOID:0111164",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111164",
            "name": "molybdenum cofactor deficiency complementation group A",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type A",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "MOCOD type A",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "MOCODA",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "molybdenum cofactor deficiency A",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "molybdenum cofactor deficiency, complementation group type a",
            "description": ""
        },
        {
            "id": "MONDO:0009643",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009643",
            "name": "molybdenum cofactor deficiency, complementation group A",
            "description": ""
        },
        {
            "id": "MIM:252150",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/252150",
            "name": "Molybdenum cofactor deficiency A",
            "description": "Molybdenum cofactor deficiency A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111164"
    ],
    "unlinked_id_list": []
}