{
    "disease_id": "DOID:0070143",
    "recommended_name": {
        "id": "DOID:0070143",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070143",
        "name": "autosomal recessive cutis laxa type III",
        "description": "A cutis laxa characterized by a progeria-like appearance, ophthalmologic abnormalities, large and late-closing fontanel, joint hyperlaxity, athetoid movements, hyperreflexia, growth retardation, intellectual deficit, developmental delay, corneal clouding, and cataract."
    },
    "synonyms": [
        {
            "id": "DOID:0070143",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070143",
            "name": "De Barsy syndrome",
            "description": ""
        },
        {
            "id": "DOID:0070143",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070143",
            "name": "cutis laxa-corneal clouding-intellectual disability syndrome",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0070132",
            "label": "autosomal recessive cutis laxa type IIIA",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070138",
            "label": "autosomal recessive cutis laxa type IIIB",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070143",
        "DOID:0070132",
        "DOID:0070138"
    ],
    "unlinked_id_list": []
}