{
    "disease_id": "DOID:0111662", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111662", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111662", 
            "name": "ECTN14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111662", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111662", 
            "name": "ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111662", 
        "description": "An ectodermal dysplasia characterized by scalp hypotrichosis and hypodontia that has_material_basis_in homozygous or compound heterozygous mutation in TSPEAR on chromosome 21q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111662", 
        "name": "ectodermal dysplasia 14"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111662#disease-associations", 
            "id": "0111662", 
            "database": "Alliance of Genome Resources"
        }
    ]
}