{
    "disease_id": "DOID:0111651", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111651", 
            "name": "ECTD15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111651", 
            "name": "ectodermal dysplasia 15, hypohidrotic/hair type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111651", 
        "description": "An ectodermal dysplasia characterized by onset in early childhood of hypotrichosis and absence of sweating except with extreme exercise that has_material_basis_in homozygous or compound heterozygous mutation in CST6 on chromosome 11q13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111651", 
        "name": "ectodermal dysplasia 15"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111651#disease-associations", 
            "id": "0111651", 
            "database": "Alliance of Genome Resources"
        }
    ]
}