{
    "disease_id": "DOID:0111394", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "Sanfilippo syndrome type B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "Mucopoly-saccharidosis type 3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "Sanfilippo B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "Sanfilippo syndrome B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "MPS3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "MPS IIIB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "mucopolysaccharidosis, type IIIB; MPS3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "N-acetyl-alpha-glucosaminidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "mucopolysaccharidosis, type IIIB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "MPS 3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "MPS III B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "mucopolysaccharidosis, type 3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "NAGLU deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "N-Acetyl-Alpha-D-glucosaminidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "MPSIIIB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009656", 
            "name": "mucopolysaccharidosis type 3B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "MPS3B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "MPSIIIB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "Mucopoly-saccharidosis type 3B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "Mucopolysaccharidosis type 3B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "N-acetyl-alpha-glucosaminidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "NAGLU deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "Sanfilippo syndrome type B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111394", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111394", 
            "name": "mucopolysaccharidosis type IIIB (Sanfilippo B)"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111394", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111394", 
        "name": "mucopolysaccharidosis type IIIB"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111394#disease-associations", 
            "id": "0111394", 
            "database": "Alliance of Genome Resources"
        }
    ]
}