{
    "disease_id": "DOID:0111389", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "Hurler-Scheie syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "Scheie disease mps type 1s"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "mucopolysaccharidosis type IH/S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "Scheie's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "MPS1H/S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "HurlerScheie syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "MPS1-HS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "mucopolysaccharidosis type 1H/S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "mucopolysaccharidosis type I-S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "l-iduronidase deficiency, Scheie type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "MPS I H-S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "MPSIH/S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "mucopolysaccharidosis type I mild form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011759", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011759", 
            "name": "mucopolysaccharidosis, mps-I-s"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111389", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111389", 
            "name": "MPS1H/S"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111389", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111389", 
            "name": "MPSIH/S"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111389", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111389", 
            "name": "Mucopolysaccharidosis type 1H/S"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111389", 
        "description": "A mucopolysaccharidosis I characterized by an intermediate severity of symptoms including short stature, corneal clouding, joint stiffening, umbilical hernia, dysostosis multiplex, hepatosplenomegaly, and little to no intellectual dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in IDUA on chromosome 4p16.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111389", 
        "name": "mucopolysaccharidosis Ih/s"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111389#disease-associations", 
            "id": "0111389", 
            "database": "Alliance of Genome Resources"
        }
    ]
}