{
    "disease_id": "DOID:0111566",
    "recommended_name": {
        "id": "DOID:0111566",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111566",
        "name": "familial isolated trichomegaly",
        "description": "An eyelid disease characterized by prolonged anagen phase of the eyelash hairs resulting in extremely long eyelashes that has_material_basis_in homozygous or compound heterozygous mutation in the FGF5 gene on chromosome 4q21.21."
    },
    "synonyms": [
        {
            "id": "DOID:0111566",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111566",
            "name": "TCMGLY",
            "description": ""
        },
        {
            "id": "DOID:0111566",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111566",
            "name": "long eyelashes",
            "description": ""
        },
        {
            "id": "MONDO:0008593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008593",
            "name": "trichomegaly",
            "description": ""
        },
        {
            "id": "MONDO:0008593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008593",
            "name": "trichomegaly",
            "description": ""
        },
        {
            "id": "MONDO:0008593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008593",
            "name": "TCMGLY",
            "description": ""
        },
        {
            "id": "MIM:190330",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/190330",
            "name": "Trichomegaly",
            "description": "Trichomegaly"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111566"
    ],
    "unlinked_id_list": []
}