{
    "disease_id": "DOID:0111167", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "DMC disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "Dyggve-Melchior-Clausen disease; DMC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "DMC syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "Dyggve-Melchior-Clausen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "DMC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009130", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009130", 
            "name": "pseudo-Morquio disease type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111167", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111167", 
            "name": "DMC disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111167", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111167", 
            "name": "pseudo-Morquio disease type I"
        }, 
        {
            "url": "https://www.omim.org/entry/223800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:223800", 
            "name": "Dyggve-Melchior-Clausen syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111167", 
        "description": "A spondyloepimetaphyseal dysplasia characterized by clawed fingers, platyspondyly of the spine, abnormalities of the iliac crest, intellectual disability and mucopolysaccharide in the urine that has_material_basis_in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111167", 
        "name": "Dyggve-Melchior-Clausen disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/223800", 
            "id": "223800", 
            "database": "MIM"
        }
    ]
}