{
    "disease_id": "DOID:0060241", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "three M syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "three M syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "three M syndrome 3; 3M3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "3M syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "CCDC8 3-M syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "3-M syndrome caused by mutation in CCDC8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013627", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013627", 
            "name": "3M3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "Le Merrer syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "Miller-McKusick-Malvaux syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "Yakut short stature syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "dolichospondylic dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "gloomy face syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060241", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060241", 
            "name": "three M syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060241", 
        "description": "A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060241", 
        "name": "3-M syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060241#disease-associations", 
            "id": "0060241", 
            "database": "Alliance of Genome Resources"
        }
    ]
}