{
    "disease_id": "DOID:0060719", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014011", 
            "name": "ARCI10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014011", 
            "name": "ichthyosis, congenital, autosomal recessive type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014011", 
            "name": "ichthyosis, congenital, autosomal recessive 10; ARCI10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014011", 
            "name": "ichthyosis, congenital, autosomal recessive 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014011", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014011", 
            "name": "autosomal recessive congenital ichthyosis type 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060719", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060719", 
            "name": "ARCI10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060719", 
        "description": "An autosomal recessive congenital ichthyosis characterized by generalized ichthyosis, moderade erythroderma, palmoplantar keratoderma and hypergranulosis that has_material_basis_in homozygous mutation in the PNPLA1 gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060719", 
        "name": "autosomal recessive congenital ichthyosis 10"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060719#disease-associations", 
            "id": "0060719", 
            "database": "Alliance of Genome Resources"
        }
    ]
}