{
    "disease_id": "DOID:0060395",
    "recommended_name": {
        "id": "DOID:0060395",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060395",
        "name": "chromosome 15q24 deletion syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060395",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060395",
            "name": "15q24 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "chromosome 15q24 deletion syndrome",
            "description": "15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies."
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "15q24 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "15q24 recurrent microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "Del(15)(q24)",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "chromosome 15q24 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "monosomy 15q24",
            "description": ""
        },
        {
            "id": "MONDO:0013256",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013256",
            "name": "WITKOS",
            "description": ""
        },
        {
            "id": "MIM:613406",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613406",
            "name": "Witteveen-Kolk syndrome",
            "description": "Witteveen-Kolk syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060395"
    ],
    "unlinked_id_list": []
}