{
    "disease_id": "DOID:0111651",
    "recommended_name": {
        "id": "DOID:0111651",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111651",
        "name": "ectodermal dysplasia 15",
        "description": "An ectodermal dysplasia characterized by onset in early childhood of hypotrichosis and absence of sweating except with extreme exercise that has_material_basis_in homozygous or compound heterozygous mutation in the CST6 gene on chromosome 11q13.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111651",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111651",
            "name": "ECTD15",
            "description": ""
        },
        {
            "id": "DOID:0111651",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111651",
            "name": "ectodermal dysplasia 15, hypohidrotic/hair type",
            "description": ""
        },
        {
            "id": "MONDO:0032804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032804",
            "name": "ectodermal dysplasia 15, hypohidrotic/hair type",
            "description": ""
        },
        {
            "id": "MONDO:0032804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032804",
            "name": "ECTD15",
            "description": ""
        },
        {
            "id": "MIM:618535",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618535",
            "name": "Ectodermal dysplasia 15, hypohidrotic/hair type",
            "description": "Ectodermal dysplasia 15, hypohidrotic/hair type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111651"
    ],
    "unlinked_id_list": []
}