{
    "disease_id": "DOID:0111393", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "Sanfilippo syndrome type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "mucopolysaccharidosis type 3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "MPSIIIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "Sanfilippo syndrome C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "Mucopoly-saccharidosis type 3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "mucopolysaccharidosis, type IIIC; MPS3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "mucopolysaccharidosis, type IIIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "Sanfilippo C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "MPS IIIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "MPS3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "MPS 3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "acetyl-CoA:alpha-glucosaminide N-acetyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "mucopolysaccharidosis, type 3C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "Acetyl-CoA alpha-glucosaminide n-acetyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "MPS III C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "heparan-alpha-glucosaminide N-acetyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009657", 
            "name": "HGSNAT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "HGSNAT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "MPS3C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "MPSIIIC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "Mucopolysaccharidosis type 3C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "Sanfilippo syndrome type C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "mucopolysaccharidosis type IIIC (Sanfilippo C)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111393", 
            "name": "Heparan-alpha-glucosaminide N-acetyltransferase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111393", 
        "description": "A mucopolysaccharidosis III that has_material_basis_in homozygous or compound heterozygous mutation in HGSNAT on chromosome 8p11.2-p11.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111393", 
        "name": "mucopolysaccharidosis type IIIC"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=138050", 
            "id": "138050", 
            "database": "GlyCosmos"
        }
    ]
}