{
    "disease_id": "DOID:0111528", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008059", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008059", 
            "name": "reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008059", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008059", 
            "name": "Nfj syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008059", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008059", 
            "name": "Naegeli syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008059", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008059", 
            "name": "NFJS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008059", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008059", 
            "name": "NAEGELI-Franceschetti-Jadassohn syndrome; NFJS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111528", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111528", 
            "name": "NFJ syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111528", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111528", 
            "name": "Naegeli syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111528", 
        "description": "A ectodermal dysplasia characterized by reticulate hyperpigmentation that made fade with age, palmoplantar keratoderma, absence of dermatoglyphics, abnormal sweat function and dental anomalies that has_material_basis_in heterozygous mutation in KRT14 on chromosome 17q21.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111528", 
        "name": "Naegeli-Franceschetti-Jadassohn syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111528#disease-associations", 
            "id": "0111528", 
            "database": "Alliance of Genome Resources"
        }
    ]
}