{
    "disease_id": "DOID:14793", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "ectodermal dysplasia and immunodeficiency 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "ectodermal dysplasia, anhidrotic, with immune deficiency 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "HED-Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "EDAID1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "ectodermal dysplasia, hypohidrotic, with immune deficiency 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0020740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0020740", 
            "name": "EDA-Id"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14793", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14793", 
            "name": "Christ-Siemens-Touraine Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14793", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14793", 
            "name": "Ectodermal Dysplasia 1, Anhydrotic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14793", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14793", 
            "name": "Hypohidrotic X-linked ectodermal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14793", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14793", 
            "name": "anhidrotic ectodermal dysplasia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14793", 
        "description": "An ectodermal dysplasia that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth).", 
        "resource": "Disease Ontology", 
        "id": "DOID:14793", 
        "name": "hypohidrotic ectodermal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14793#disease-associations", 
            "id": "14793", 
            "database": "Alliance of Genome Resources"
        }
    ]
}