{
    "disease_id": "DOID:0111394",
    "recommended_name": {
        "id": "DOID:0111394",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111394",
        "name": "mucopolysaccharidosis type IIIB",
        "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "MPS3B",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "MPSIIIB",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "Mucopoly-saccharidosis type 3B",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "Mucopolysaccharidosis type 3B",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "N-acetyl-alpha-glucosaminidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "NAGLU deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "Sanfilippo syndrome type B",
            "description": ""
        },
        {
            "id": "DOID:0111394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111394",
            "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "mucopolysaccharidosis type 3B",
            "description": "A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetyl-alpha-D-glucosaminidase. It is characterized by behavioral changes, sleep disturbances, and mental developmental delays."
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "MPS III B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "MPS3B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "MPSIIIB",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "N-acetyl-alpha-glucosaminidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "Sanfilippo B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "Sanfilippo syndrome B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "Sanfilippo syndrome type B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "mucopolysaccharidosis type 3B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "mucopolysaccharidosis type IIIB",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "MPS IIIB",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "Mucopoly-saccharidosis type 3B",
            "description": ""
        },
        {
            "id": "MONDO:0009656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009656",
            "name": "mucopolysaccharidosis, type IIIB",
            "description": ""
        },
        {
            "id": "MIM:252920",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/252920",
            "name": "Mucopolysaccharidosis 3B",
            "description": "Mucopolysaccharidosis 3B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111394"
    ],
    "unlinked_id_list": []
}