{
    "disease_id": "DOID:0111528",
    "recommended_name": {
        "id": "DOID:0111528",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111528",
        "name": "Naegeli-Franceschetti-Jadassohn syndrome",
        "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 the KRT14 gene on chromosome 17q21.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111528",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111528",
            "name": "NFJ syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111528",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111528",
            "name": "Naegeli syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "Naegeli-Franceschetti-Jadassohn syndrome",
            "description": "Naegeli-Franceschetti-Jadassohn (NFJ) syndrome is a rare ectodermal dysplasia that affects the skin, sweat glands, nails, and teeth."
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "NFJ syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "Naegeli syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "Naegeli-Franceschetti-Jadassohn syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "NFJS",
            "description": ""
        },
        {
            "id": "MONDO:0008059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008059",
            "name": "reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy",
            "description": ""
        },
        {
            "id": "MIM:161000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/161000",
            "name": "Naegeli-Franceschetti-Jadassohn syndrome",
            "description": "Naegeli-Franceschetti-Jadassohn syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111528"
    ],
    "unlinked_id_list": []
}