{
    "disease_id": "DOID:0060428", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "chromosome 2q32-q33 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "SATB2 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "monosomy 2q32-q33"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "glass"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "monosomy 2q32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "glass syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "2q32q33 microdeletion syndromes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "SAS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "glass syndrome; glass"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "monosomy 2q32q33"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "Del(2)(q32q33)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "2q32-q33 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "Del(2)(q32)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012864", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012864", 
            "name": "2q32q33 microdeletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "chromosome 2q32-q33 deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "2q32-q33 microdeletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "2q32q33 microdeletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "Glass syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "monosomy 2q32"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "monosomy 2q32-q33"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060428", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060428", 
            "name": "monosomy 2q32q33"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060428", 
        "description": "A syndrome that has_material_basis_in genetic changes that affect the SATB2 gene and that is characterized by mild to severe intellectual disability, a delayed or absent ability to speak,  severe speech anomalies, abnormalities of the palate, teeth anomalies, behavioral issues with or without bone or brain anomalies, and onset before age 2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060428", 
        "name": "SATB2-associated syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060428#disease-associations", 
            "id": "0060428", 
            "database": "Alliance of Genome Resources"
        }
    ]
}