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