{
    "disease_id": "DOID:0060419",
    "recommended_name": {
        "id": "DOID:0060419",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060419",
        "name": "chromosome 3q29 microdeletion syndrome",
        "description": "A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 3q29 region."
    },
    "synonyms": [
        {
            "id": "DOID:0060419",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060419",
            "name": "3q subtelomere deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060419",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060419",
            "name": "3q29 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060419",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060419",
            "name": "3qter deletion",
            "description": ""
        },
        {
            "id": "DOID:0060419",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060419",
            "name": "3q29 recurrent deletion",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "chromosome 3q29 microdeletion syndrome",
            "description": "3q29 microdeletion syndrome is a recurrent subtelomeric deletion syndrome with variable clinical manifestations including intellectual deficit and dysmorphic features."
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "3qter deletion",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "monosomy 3qter",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "3q29 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "3q29 deletion",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "monosomy 3q29",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "chromosome 3q29 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "3q29 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "microdeletion 3Q29 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "3q subtelomere deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012269",
            "name": "Del(3)(q29)",
            "description": ""
        }
    ]
}