{
    "disease_id": "DOID:0111665", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009147", 
            "name": "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009147", 
            "name": "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive; ECTD10B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009147", 
            "name": "ectodermal dysplasia, hypohidrotic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009147", 
            "name": "ectodermal dysplasia, anhidrotic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009147", 
            "name": "ECTD10B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111665", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111665", 
            "name": "ECTD10B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111665", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111665", 
            "name": "ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive"
        }, 
        {
            "url": "https://www.omim.org/entry/224900", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:224900", 
            "name": "Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111665", 
        "description": "A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in EDAR on chromosome 2q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111665", 
        "name": "ectodermal dysplasia 10B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/224900", 
            "id": "224900", 
            "database": "MIM"
        }
    ]
}