{
    "disease_id": "DOID:0111392",
    "recommended_name": {
        "id": "DOID:0111392",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111392",
        "name": "mucopolysaccharidosis type IVB",
        "description": "A mucopolysaccharidosis IV characterized by skeletal dysplasia, corneal clouding, and increased urinary keratan sulfate excretion that has_material_basis_in homozygous or compound heterozygous mutation in the GLB1 gene on chromosome 3p22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "MPS IVB",
            "description": ""
        },
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "MPS4B",
            "description": ""
        },
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "Morquio disease type B",
            "description": ""
        },
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "Morquio syndrome B",
            "description": ""
        },
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "beta-D-galactosidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111392",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111392",
            "name": "mucopolysaccharidosis type IVB (Morquio)",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "mucopolysaccharidosis type 4B",
            "description": "A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme beta galactosidase. It is characterized by skeletal dysplasia and short stature."
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "Beta-D-galactosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "MPS 4B",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "MPS IV B",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "MPS4B",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "MPSIVB",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "Morquio disease type B",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "Morquio syndrome B",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "mucopolysaccharidosis type IVB",
            "description": ""
        },
        {
            "id": "MONDO:0009660",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009660",
            "name": "MPS IVB",
            "description": ""
        },
        {
            "id": "MIM:253010",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/253010",
            "name": "Mucopolysaccharidosis 4B",
            "description": "Mucopolysaccharidosis 4B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111392"
    ],
    "unlinked_id_list": []
}