{
    "disease_id": "DOID:0060289",
    "recommended_name": {
        "id": "DOID:0060289",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060289",
        "name": "Ohdo syndrome",
        "description": "A syndrome that is characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability."
    },
    "synonyms": [
        {
            "id": "DOID:0060289",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060289",
            "name": "Ohdo blepharophimosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "blepharophimosis - intellectual disability syndrome, Ohdo type",
            "description": "Ohdo blepharophimosis syndrome (OBS) is a multiple congenital malformation syndrome characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability."
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "BMRS, Ohdo type",
            "description": ""
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "Ohdo syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "Ohdo-Madokoro-Sonoda syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "blepharophimosis syndrome, Ohdo type",
            "description": ""
        },
        {
            "id": "MONDO:0009583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009583",
            "name": "mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "blepharophimosis - intellectual disability syndrome, MKB type",
            "description": "The Maat-Kievit-Brunner type of Ohdo syndrome is a rare condition characterized by intellectual disability and distinctive facial features. It has only been reported in males."
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "BMRS, MKB type",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "BMRS, Maat-Kievit-Brunner type",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "Ohdo syndrome, X-linked, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "X-linked Ohdo syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "OHDOX",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "Ohdo syndrome, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010477",
            "name": "blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type",
            "description": ""
        },
        {
            "id": "MIM:300895",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300895",
            "name": "Ohdo syndrome, X-linked",
            "description": "Ohdo syndrome, X-linked"
        }
    ],
    "children": [
        {
            "id": "DOID:0060290",
            "label": "Ohdo syndrome, SBBYS variant",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060289",
        "DOID:0060290"
    ],
    "unlinked_id_list": []
}