{
    "disease_id": "DOID:11486",
    "recommended_name": {
        "id": "DOID:11486",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:11486",
        "name": "Horner's syndrome",
        "description": "An autonomic neuropathy that is characterized by the classic triad of unilateral ptosis, unilateral miosis with anisocoria, and ipsilateral facial anhidrosis, resulting from unilateral paralysis of the cervical sympathetics."
    },
    "synonyms": [
        {
            "id": "DOID:11486",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11486",
            "name": "Bernard Horner syndrome",
            "description": ""
        },
        {
            "id": "DOID:11486",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11486",
            "name": "Horner syndrome",
            "description": ""
        },
        {
            "id": "DOID:11486",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11486",
            "name": "cervical sympathetic paralysis",
            "description": ""
        },
        {
            "id": "MONDO:0007735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007735",
            "name": "congenital Horner syndrome",
            "description": "Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported."
        },
        {
            "id": "MONDO:0007735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007735",
            "name": "congenital Claude-Bernard-Horner syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007735",
            "name": "congenital Horner syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007735",
            "name": "congenital Horner syndrome (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0007735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007735",
            "name": "HORNER syndrome, congenital",
            "description": ""
        }
    ]
}