{
    "disease_id": "DOID:0050657", 
    "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:0050657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050657", 
            "name": "Bannayan-Zonana syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050657", 
            "name": "Riley-Smith syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050657", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050657", 
            "name": "Ruvalcaba-Myhre-Smith syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050657", 
        "description": "A syndrome that is characterized by macrocephaly, multiple noncancerous tumors and hamartomas, and dark freckles on the penis, and has_material_basis_in heterozygous germline mutation in the PTEN gene on chromosome 10q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050657", 
        "name": "Bannayan-Riley-Ruvalcaba syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050657#disease-associations", 
            "id": "0050657", 
            "database": "Alliance of Genome Resources"
        }
    ]
}