{
    "disease_id": "DOID:0111167",
    "recommended_name": {
        "id": "DOID:0111167",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111167",
        "name": "Dyggve-Melchior-Clausen disease",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111167",
            "name": "DMC disease",
            "description": ""
        },
        {
            "id": "DOID:0111167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111167",
            "name": "pseudo-Morquio disease type I",
            "description": ""
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "Dyggve-Melchior-Clausen disease",
            "description": "Dyggve-Melchior-Clausen disease (DMC) is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias."
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "Dyggve Melchior Clausen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "Dyggve-Melchior-Clausen disease",
            "description": ""
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "Dyggve-Melchior-Clausen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "DMC",
            "description": ""
        },
        {
            "id": "MONDO:0009130",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009130",
            "name": "DMC syndrome",
            "description": ""
        },
        {
            "id": "MIM:223800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/223800",
            "name": "Dyggve-Melchior-Clausen syndrome",
            "description": "Dyggve-Melchior-Clausen syndrome"
        }
    ],
    "children": [
        {
            "id": "DOID:0060247",
            "label": "Smith-McCort dysplasia",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0081270",
                    "label": "Smith-McCort dysplasia 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081271",
                    "label": "Smith-McCort dysplasia 2",
                    "link_status": true,
                    "children": []
                }
            ]
        }
    ],
    "id_list": [
        "DOID:0060247",
        "DOID:0111167",
        "DOID:0081270",
        "DOID:0081271"
    ],
    "unlinked_id_list": []
}