{
    "disease_id": "DOID:0060714", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "type 3 lamellar ichthyosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, congenital, autosomal recessive type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis congenita III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis congenita 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, Nonlamellar and Nonerythrodermic, congenital, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, congenital, autosomal recessive 5; ARCI5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis lamellar 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "autosomal recessive congenital ichthyosis type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, lamellar, 3, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "LI3, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, lamellar, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ARCI5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "NNCI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "ichthyosis, congenital, autosomal recessive 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011485", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011485", 
            "name": "lamellar ichthyosis, type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060714", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060714", 
            "name": "autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060714", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060714", 
            "name": "ARCI5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060714", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060714", 
        "name": "autosomal recessive congenital ichthyosis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060714#disease-associations", 
            "id": "0060714", 
            "database": "Alliance of Genome Resources"
        }
    ]
}