{
    "disease_id": "DOID:0060247", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "Smith-McCort dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "SMC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "Smith-McCort dysplasia caused by mutation in DYM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "Smc1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "Smith-McCort dysplasia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "SMITH-McCort dysplasia 1; Smc1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011814", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011814", 
            "name": "DYM Smith-McCort dysplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/607326", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607326", 
            "name": "Smith-McCort dysplasia 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060247", 
        "description": "A Syggve-Melchior-Clausen disease characterized by short limbs and a short trunk with a barrel-shaped chest and has_material_basis_in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060247", 
        "name": "Smith-McCort dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607326", 
            "id": "607326", 
            "database": "MIM"
        }
    ]
}