{
    "disease_id": "DOID:0060710", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "Brocq congenital ichthyosiform erythroderma nonbullous form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosis, congenital, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "NCIE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosis, congenital, autosomal recessive type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "nonbullous congenital ichthyosiform erythroderma 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "NCIE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosis, congenital, autosomal recessive 2; ARCI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosiform erythroderma, congenital, nonbullous, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosiform erythroderma, Brocq congenital, nonbullous form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosiform erythroderma, nonbullous congenital, 1, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "NBCIE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "autosomal recessive congenital ichthyosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ichthyosiform erythroderma, nonbullous congenital, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "ARCI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009439", 
            "name": "collodion baby, self-healing"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060710", 
            "name": "ARCI2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060710", 
            "name": "NCIE1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060710", 
            "name": "nonbullous congenital ichthyosiform erythroderma 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060710", 
            "name": "BROCQ congenital ichthyosiform erythroderma nonbullous form"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060710", 
        "description": "An autosomal recessive congenital ichthyosis characterized by fine scales on the scalp, face, trunk and limbs, marked palmoplantar hyperlinearity, hyperkeratosis, acanthosis, mild hypergranulosis and thickened stratum corneum that has_material_basis_in homozygous or compound heterozygous mutation in the ALOX12B gene on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060710", 
        "name": "autosomal recessive congenital ichthyosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060710#disease-associations", 
            "id": "0060710", 
            "database": "Alliance of Genome Resources"
        }
    ]
}