{
    "disease_id": "DOID:0061145",
    "recommended_name": {
        "id": "DOID:0061145",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061145",
        "name": "monilethrix 1",
        "description": "A hair disease that is characterized by beading of the hair shaft caused by periodic constrictions and that has_material_basis_in heterozygous mutation in the hair cortex keratin gene KRT86 on chromosome 12q13."
    },
    "synonyms": [
        {
            "id": "DOID:0061145",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061145",
            "name": "MNLIX1",
            "description": ""
        },
        {
            "id": "MONDO:0700343",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0700343",
            "name": "monilethrix-1",
            "description": ""
        },
        {
            "id": "MIM:158000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/158000",
            "name": "Monilethrix 1",
            "description": "Monilethrix 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061145"
    ],
    "unlinked_id_list": []
}
