{
    "disease_id": "DOID:0060720",
    "recommended_name": {
        "id": "DOID:0060720",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060720",
        "name": "autosomal recessive congenital ichthyosis 11",
        "description": "An autosomal recessive congenital ichthyosis characterized by ichthyosis, hypotrichosis, photophobia, corneal opacity, pingueculum, blepharitis, marked acanthosis, otrhohyperkeratosis and hyperkeratosis that has_material_basis_in homozygous mutation in the ST14 gene on chromosome 11q24."
    },
    "synonyms": [
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            "description": ""
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            "description": ""
        },
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            "id": "MONDO:0011218",
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            "description": ""
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            "description": "Ichthyosis, congenital, autosomal recessive 11"
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    ],
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    "id_list": [
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            "id": "DOID:0060720",
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            "categories": []
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                    "name": "wu:fi41g07",
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                    "name": "Rattus norvegicus",
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}