{
    "disease_id": "DOID:0111653",
    "recommended_name": {
        "id": "DOID:0111653",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111653",
        "name": "ectodermal dysplasia 11A",
        "description": "A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in the EDARADD gene on chromosome 1q42-q43."
    },
    "synonyms": [
        {
            "id": "DOID:0111653",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111653",
            "name": "ECTD11A",
            "description": ""
        },
        {
            "id": "DOID:0111653",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111653",
            "name": "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013982",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013982",
            "name": "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013982",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013982",
            "name": "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013982",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013982",
            "name": "ECTD11A",
            "description": ""
        },
        {
            "id": "MONDO:0013982",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013982",
            "name": "ectodermal dysplasia, hypohidrotic, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:614940",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614940",
            "name": "Ectodermal dysplasia 11A, hypohidrotic/hair/nail type, autosomal dominant",
            "description": "Ectodermal dysplasia 11A, hypohidrotic/hair/nail type, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111653"
    ],
    "unlinked_id_list": []
}