{
    "disease_id": "DOID:0060395", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "monosomy 15q24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "Del(15)(q24)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "15q24 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "Witteveen-Kolk syndrome; WITKOS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "WITKOS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "chromosome 15Q24 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013256", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013256", 
            "name": "Witteveen-Kolk syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060395", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060395", 
            "name": "15q24 microdeletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060395", 
        "description": "A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060395", 
        "name": "chromosome 15q24 deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060395#disease-associations", 
            "id": "0060395", 
            "database": "Alliance of Genome Resources"
        }
    ]
}