{
    "disease_id": "DOID:0080143", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "congenital fibrosis of extraocular muscles type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "fibrosis of extraocular muscles, congenital, 3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "fibrosis of extraocular muscles, congenital, 1; CFEOM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "fibrosis of extraocular muscles, congenital, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "CFEOM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "congenital fibrosis of extraocular muscles caused by mutation in KIF21A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "KIF21A congenital fibrosis of extraocular muscles"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "ophthalmoplegia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "blepharoptosis with absent eye movements"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021083", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021083", 
            "name": "Feom1 locus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080143", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080143", 
            "name": "Tukel syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/135700", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:135700", 
            "name": "Fibrosis of extraocular muscles, congenital, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080143", 
        "description": "An ocular motility disease that is characterized by the inability to move the eyes in certain directions, droopy eyelids and eyes that are fixed in an abnormal position.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080143", 
        "name": "congenital fibrosis of the extraocular muscles"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/135700", 
            "id": "135700", 
            "database": "MIM"
        }
    ]
}