{
    "disease_id": "DOID:0111553", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008473", 
            "name": "spondyloepiphyseal dysplasia, Maroteaux type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008473", 
            "name": "pseudo-Morquio syndrome, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008473", 
            "name": "brachyolmia Maroteaux type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008473", 
            "name": "pseudo-Morquio syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008473", 
            "name": "Sed, Maroteaux type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111553", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111553", 
            "name": "Brachyolmia Type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111553", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111553", 
            "name": "Pseudo-Morquio syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111553", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111553", 
            "name": "SED, Maroteaux type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111553", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111553", 
            "name": "spondyloepiphyseal dysplasia of Maroteaux"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111553", 
        "description": "An osteochondrodysplasia characterized by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, platyspondyly, severe brachydactyly, and pelvic abnormalities that has_material_basis_in heterozygous mutation in TRPV4 on chromosome 12q24.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111553", 
        "name": "spondyloepiphyseal dysplasia Maroteaux type"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/184095", 
            "id": "184095", 
            "database": "MIM"
        }
    ]
}