{
    "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:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "Horner syndrome",
            "description": "Horner's syndrome is a rare condition characterized by miosis (constriction of thepupil), ptosis (drooping of the upper eyelid), and anhidrosis (absence of sweating of the face). It iscaused by damage to the sympathetic nerves of the face. The underlying causes of Horner's syndrome vary greatly and may include a tumor, stroke, or other damage to a part of the brain called the brain stem ; injury to the carotid artery ;and trauma to the brachial plexus. In rare cases, Horner's syndrome is congenital (present from birth) and associated with a lack of pigmentation of the iris (colored part of the eye). Treatment of Horner's syndrome depends on the underlying cause."
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "Horner's syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "Horner syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "oculosympathetic palsy",
            "description": ""
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "cervical sympathetic paralysis",
            "description": ""
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "Bernard-Horner syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0001294",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0001294",
            "name": "Bernard Horner syndrome",
            "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": "HORNER syndrome, congenital",
            "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": "congenital Claude-Bernard-Horner syndrome",
            "description": ""
        }
    ]
}