{
    "disease_id": "DOID:0111822", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "congenital hemidysplasia with ichthyosiform nevus and limbs defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "ichthyosis, child syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "child nevus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "congenital hemidysplasia with ichthyosiform erythroderma and limb defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010621", 
            "name": "congenital hemidysplasia with ichthyosiform nevus and limb defects"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111822", 
            "name": "CHILD nevus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111822", 
            "name": "congenital hemidysplasia with ichthyosiform nevus and limbs defects"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111822", 
        "description": "A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in NSDHL on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111822", 
        "name": "CHILD syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111822#disease-associations", 
            "id": "0111822", 
            "database": "Alliance of Genome Resources"
        }
    ]
}