{
    "disease_id": "DOID:0060389",
    "recommended_name": {
        "id": "DOID:0060389",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060389",
        "name": "chromosome 10q23 deletion syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "chromosome 10q23 deletion syndrome",
            "description": "10q22.3q23.3 microdeletion syndrome is a rare partial autosomal monosomy characterized by a mild facial dysmorphism variably including macrocephaly, broad forehead, hypertelorism or hypotelorism, deep-set eyes, upslanting or downslanting palpebral fissures, low-set ears, flat nasal bridge, smooth philtrum, thin upper lip), cleft palate, cerebellar and cardiac malformations, psychomotor development delay, and behavioral abnormalities (attention deficit hyperactivity disorder, autism). Other rare features may include congenital breast aplasia, arachnodactyly, joint hyperlaxity, club feet, feeding difficulties, failure to thrive."
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "Del(10)(q22.3q23.3)",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "chromosome 10q23 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "deletion 10q22.3q23.3",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "monosomy 10q22.3q23.3",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "10q22.3q23 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "10q22.3q23.3 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "chromosome 10Q22.3-q23.2 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "chromosome 10q22.3-q23.2 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "juvenile polyposis of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0012830",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012830",
            "name": "juvenile polyposis, infantile",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060389"
    ],
    "unlinked_id_list": []
}