{
    "disease_id": "DOID:0060714",
    "recommended_name": {
        "id": "DOID:0060714",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060714",
        "name": "autosomal recessive congenital ichthyosis 5",
        "description": "An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has_material_basis_in homozygous mutation in the CYP4F22 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0060714",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060714",
            "name": "autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis",
            "description": ""
        },
        {
            "id": "DOID:0060714",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060714",
            "name": "ARCI5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "autosomal recessive congenital ichthyosis 5",
            "description": "An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has material basis in homozygous mutation in the CYP4F22 gene on chromosome 19p13."
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ARCI5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "autosomal recessive congenital ichthyosis 5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "autosomal recessive congenital ichthyosis type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis, congenital, autosomal recessive type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "LI3, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "NNCI",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis congenita 3",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis congenita III",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis lamellar 3",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis, NONLAMELLAR and NONERYTHRODERMIC, congenital, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis, congenital, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis, lamellar, 3",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "ichthyosis, lamellar, 3, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "lamellar ichthyosis, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011485",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011485",
            "name": "type 3 lamellar ichthyosis",
            "description": ""
        },
        {
            "id": "MIM:604777",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604777",
            "name": "Ichthyosis, congenital, autosomal recessive 5",
            "description": "Ichthyosis, congenital, autosomal recessive 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060714"
    ],
    "unlinked_id_list": []
}