{
    "disease_id": "DOID:0111163",
    "recommended_name": {
        "id": "DOID:0111163",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111163",
        "name": "molybdenum cofactor deficiency type B",
        "description": "A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11."
    },
    "synonyms": [
        {
            "id": "DOID:0111163",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111163",
            "name": "molybdenum cofactor deficiency complementation group B",
            "description": ""
        },
        {
            "id": "DOID:0111163",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111163",
            "name": "MOCOD type B",
            "description": ""
        },
        {
            "id": "DOID:0111163",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111163",
            "name": "MOCODB",
            "description": ""
        },
        {
            "id": "DOID:0111163",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111163",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B",
            "description": ""
        },
        {
            "id": "DOID:0111163",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111163",
            "name": "molybdenum cofactor deficiency type B1",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "MOCOD type B",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "MOCODB",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "molybdenum cofactor deficiency B",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "molybdenum cofactor deficiency, complementation group type B",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type B",
            "description": ""
        },
        {
            "id": "MONDO:0009644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009644",
            "name": "molybdenum cofactor deficiency, complementation group B",
            "description": ""
        },
        {
            "id": "MIM:252160",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/252160",
            "name": "Molybdenum cofactor deficiency B",
            "description": "Molybdenum cofactor deficiency B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111163"
    ],
    "unlinked_id_list": []
}