{
    "disease_id": "DOID:0060614", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008411", 
            "name": "ums"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008411", 
            "name": "ulnar-mammary syndrome; ums"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008411", 
            "name": "Schinzel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008411", 
            "name": "ulnar-mammary syndrome of Pallister"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008411", 
            "name": "Pallister ulnar-mammary syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060614", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060614", 
            "name": "Pallister ulnar-mammary syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060614", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060614", 
            "name": "Schinzel syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060614", 
        "description": "A syndrome that is characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and, or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies and that has_material_basis_in heterozygous mutation in the TBX3 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060614", 
        "name": "ulnar-mammary syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/181450", 
            "id": "181450", 
            "database": "MIM"
        }
    ]
}