{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Cowden syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Proteus-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Lhermitte-Duclos disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Cowden syndrome 1; CWS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Cowden syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "PTEN Cowden disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "CS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "cerebelloparenchymal disorder 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "dysplastic gangliocytoma of the cerebellum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "multiple hamartoma syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "Cowden disease caused by mutation in PTEN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "CWS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008021", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008021", 
            "name": "cerebellar granule cell Hypertrophy and megalencephaly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6457", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6457", 
            "name": "Cowden disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6457", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6457", 
            "name": "Lhermitte-Duclos disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:6457", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:6457", 
            "name": "dysplastic Gangliocytoma of Cerebellum"
        }, 
        {
            "url": "https://www.omim.org/entry/158350", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:158350", 
            "name": "Cowden syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:6457", 
        "description": "A syndrome characterized by multiple noncancerous, tumor-like growths (hamartomas) and an increased risk of certain forms of cancer, especially breast, thyroid and endometrium.", 
        "resource": "Disease Ontology", 
        "id": "DOID:6457", 
        "name": "Cowden syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/158350", 
            "id": "158350", 
            "database": "MIM"
        }
    ]
}