{
    "disease_id": "DOID:0060389", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "10q22.3q23.3 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "juvenile polyposis, infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "monosomy 10q22.3q23.3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "deletion 10q22.3q23.3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "10q22.3q23 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "chromosome 10q22.3-q23.2 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "Del(10)(q22.3q23.3)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012830", 
            "name": "juvenile polyposis of infancy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060389", 
        "description": "A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060389", 
        "name": "chromosome 10q23 deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060389#disease-associations", 
            "id": "0060389", 
            "database": "Alliance of Genome Resources"
        }
    ]
}