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