{
    "disease_id": "DOID:0070303", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia, multiple, 1; EDM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "multiple epiphyseal dysplasia (disease) caused by mutation in COMP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "Polyepiphyseal dysplasia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "multiple epiphyseal dysplasia COMP-related"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "MED1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia, ribbing type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "COMP multiple epiphyseal dysplasia (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "EDM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "multiple epiphyseal dysplasia, Comp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia, Fairbank type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia multiple 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia, multiple, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007561", 
            "name": "epiphyseal dysplasia, multiple, 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070303", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070303", 
            "name": "EDM1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070303", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070303", 
            "name": "MED1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070303", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070303", 
            "name": "multiple epiphyseal dysplasia COMP-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070303", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070303", 
            "name": "polyepiphyseal dysplasia type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070303", 
        "description": "A multiple epiphyseal dysplasia that has_material_basis_in heterozygous mutation in the COMP gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070303", 
        "name": "multiple epiphyseal dysplasia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/132400", 
            "id": "132400", 
            "database": "MIM"
        }
    ]
}