{
    "disease_id": "DOID:2121", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2121", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2121", 
            "name": "Congenital ectodermal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2121", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2121", 
            "name": "Congenital ectodermal defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ectodysplasin.", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "X-linked hypohidrotic ectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "hypohidrotic ectodermal dysplasia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "hypohidrotic ectodermal dysplasia X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia 1, hypohidrotic, X-linked; XHED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "CST syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia 1, hypohidrotic, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "anhidrotic ectodermal dysplasia X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "XHED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "Christ-Siemens-Touraine syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "Eda1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia, anhidrotic, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia 1, hypohidrotic/hair/Tooth type, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "Xlhed"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "ectodermal dysplasia, hypohidrotic, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010585", 
            "name": "X-linked anhidrotic ectodermal dysplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/305100", 
            "description": "Ectodermal dysplasia 1, hypohidrotic, X-linked", 
            "resource": "MIM", 
            "id": "MIM:305100", 
            "name": "Ectodermal dysplasia 1, hypohidrotic, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2121", 
        "description": "A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2121", 
        "name": "ectodermal dysplasia"
    }
}