{
    "disease_id": "DOID:0111652",
    "recommended_name": {
        "id": "DOID:0111652",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111652",
        "name": "ectodermal dysplasia 12",
        "description": "A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in the KDF1 gene on chromosome 1p36.11."
    },
    "synonyms": [
        {
            "id": "DOID:0111652",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111652",
            "name": "ECTD12",
            "description": ""
        },
        {
            "id": "DOID:0111652",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111652",
            "name": "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type",
            "description": ""
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type",
            "description": "Any ectodermal dysplasia syndrome in which the cause of the disease is a mutation in the KDF1 gene."
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "ECTD12",
            "description": ""
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "KDF1 ectodermal dysplasia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "ectodermal dysplasia 12, hypohidrotic/hair/Tooth/nail type",
            "description": ""
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type; ECTD12",
            "description": ""
        },
        {
            "id": "MONDO:0015024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015024",
            "name": "ectodermal dysplasia syndrome caused by mutation in KDF1",
            "description": ""
        },
        {
            "id": "MIM:617337",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617337",
            "name": "Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type",
            "description": "Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111652"
    ],
    "unlinked_id_list": []
}