{
    "disease_id": "DOID:0060718", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014010", 
            "name": "ARCI9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014010", 
            "name": "ichthyosis, congenital, autosomal recessive type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014010", 
            "name": "ichthyosis, congenital, autosomal recessive 9; ARCI9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014010", 
            "name": "autosomal recessive congenital ichthyosis type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014010", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014010", 
            "name": "ichthyosis, congenital, autosomal recessive 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060718", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060718", 
            "name": "ARCI9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060718", 
        "description": "An autosomal recessive congenital ichthyosis characterized by fine erythrodermic scales, palmoplantar hyperlinearity, thick orthohyperkeratosis, hypergranulosis, moderate acanthosis and mild alopecia that has_material_basis_in homozygous mutation in the CERS3 gene on chromosome 15q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060718", 
        "name": "autosomal recessive congenital ichthyosis 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060718#disease-associations", 
            "id": "0060718", 
            "database": "Alliance of Genome Resources"
        }
    ]
}