{
    "disease_id": "DOID:0111871",
    "recommended_name": {
        "id": "DOID:0111871",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111871",
        "name": "photosensitive trichothiodystrophy 3",
        "description": "A photosensitive trichothiodystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the GTF2H5 gene on chromosome 6q25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111871",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111871",
            "name": "TTD3",
            "description": ""
        },
        {
            "id": "DOID:0111871",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111871",
            "name": "trichothiodystrophy complementation group A",
            "description": ""
        },
        {
            "id": "MONDO:0014619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014619",
            "name": "trichothiodystrophy 3, photosensitive",
            "description": ""
        },
        {
            "id": "MONDO:0014619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014619",
            "name": "trichothiodystrophy 3, photosensitive",
            "description": ""
        },
        {
            "id": "MONDO:0014619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014619",
            "name": "TTD3",
            "description": ""
        },
        {
            "id": "MIM:616395",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616395",
            "name": "Trichothiodystrophy 3, photosensitive",
            "description": "Trichothiodystrophy 3, photosensitive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111871"
    ],
    "unlinked_id_list": []
}