{
    "disease_id": "DOID:0060711",
    "recommended_name": {
        "id": "DOID:0060711",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060711",
        "name": "autosomal recessive congenital ichthyosis 3",
        "description": "An autosomal recessive congenital ichthyosis characterized by mild ichthyosis, fine scales on the scalp, face, trunk and limbs, dark brown adherent scales on the neck, elbow and knees, and hypohydrosis that has_material_basis_in homozygous or compound heterozygous mutation in the ALOXE3 gene on chromosome 17p13."
    },
    "synonyms": [
        {
            "id": "DOID:0060711",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060711",
            "name": "ARCI3",
            "description": ""
        },
        {
            "id": "DOID:0060711",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060711",
            "name": "lamellar ichthyosis 5",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "autosomal recessive congenital ichthyosis 3",
            "description": "Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the ALOXE3 gene."
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ARCI3",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "collodion baby, self-healing",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ichthyosis, lamellar, 5, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ichthyosis, congenital, autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "autosomal recessive congenital ichthyosis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ichthyosis, lamellar, 5",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "lamellar ichthyosis 5",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ichthyosis, congenital, autosomal recessive type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011680",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011680",
            "name": "ichthyosis, congenital, autosomal recessive 3; ARCI3",
            "description": ""
        },
        {
            "id": "MIM:606545",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606545",
            "name": "Ichthyosis, congenital, autosomal recessive 3",
            "description": "Ichthyosis, congenital, autosomal recessive 3"
        }
    ]
}