{
    "disease_id": "DOID:0111660", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013975", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013975", 
            "name": "ectodermal dysplasia 7, hair/nail type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013975", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013975", 
            "name": "KRT74 pure hair and nail ectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013975", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013975", 
            "name": "pure hair and nail ectodermal dysplasia caused by mutation in KRT74"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013975", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013975", 
            "name": "ECTD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013975", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013975", 
            "name": "ectodermal dysplasia 7, hair/nail type; ECTD7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111660", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111660", 
            "name": "ECTD7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111660", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111660", 
            "name": "ectodermal dysplasia 7, hair/nail type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111660", 
        "description": "A pure hair and nail ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in KRT74 on chromosome 12q13.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111660", 
        "name": "ectodermal dysplasia 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111660#disease-associations", 
            "id": "0111660", 
            "database": "Alliance of Genome Resources"
        }
    ]
}