{
    "disease_id": "DOID:0111654", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013983", 
            "name": "ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013983", 
            "name": "ECTD11B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013983", 
            "name": "ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive; ECTD11B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013983", 
            "name": "ectodermal dysplasia, hypohidrotic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013983", 
            "name": "ectodermal dysplasia, anhidrotic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111654", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111654", 
            "name": "ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111654", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111654", 
            "name": "ECTD11B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111654", 
        "description": "A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in EDARADD on chromosome 1q42-q43.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111654", 
        "name": "ectodermal dysplasia 11B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111654#disease-associations", 
            "id": "0111654", 
            "database": "Alliance of Genome Resources"
        }
    ]
}