{
    "disease_id": "DOID:0060289", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "blepharophimosis - intellectual disability syndrome, MKB type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "Ohdo syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "X-linked Ohdo syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "Ohdo syndrome, X-linked; OHDOX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "BMRS, MKB type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "OHDOX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010477", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010477", 
            "name": "BMRS, Maat-Kievit-Brunner type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060289", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060289", 
            "name": "Ohdo blepharophimosis syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/300895", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300895", 
            "name": "Ohdo syndrome, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060289", 
        "description": "A syndrome that is characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060289", 
        "name": "Ohdo syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300895", 
            "id": "300895", 
            "database": "MIM"
        }
    ]
}