{
    "disease_id": "DOID:0060810",
    "recommended_name": {
        "id": "DOID:0060810",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060810",
        "name": "syndromic X-linked intellectual disability type 10",
        "description": "A syndromic X-linked intellectual disability characterized by mild intellectual deficit associated with choreoathetosis and abnormal behaviour that has_material_basis_in mutation in the HSD17B10 gene on chromosome Xp11.22."
    },
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            "description": ""
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            "name": "HSD10 disease, atypical type",
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        },
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            "description": ""
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            "name": "3-hydroxyacyl-CoA dehydrogenase 2 deficiency",
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            "name": "17 beta-hydroxysteroid dehydrogenase type 10 deficiency",
            "description": ""
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            "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency",
            "description": ""
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        {
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            "name": "hydroxyacyl-CoA dehydrogenase II deficiency",
            "description": ""
        },
        {
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            "resource": "MIM",
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            "name": "HSD10 mitochondrial disease",
            "description": "HSD10 mitochondrial disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060810"
    ],
    "unlinked_id_list": []
}