{
    "disease_id": "DOID:0111361",
    "recommended_name": {
        "id": "DOID:0111361",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111361",
        "name": "hypotrichosis-lymphedema-telangiectasia syndrome",
        "description": "A syndrome characterized by onset at birth or early childhood of progressive hypotrichosis, lymphedema, and telangiectasia that has_material_basis_in homozygous or compound heterozygous mutation in the SOX18 gene on chromosome 20q13.33."
    },
    "synonyms": [
        {
            "id": "DOID:0111361",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111361",
            "name": "HLTS",
            "description": ""
        },
        {
            "id": "MONDO:0011914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011914",
            "name": "hypotrichosis-lymphedema-telangiectasia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011914",
            "name": "hypotrichosis-lymphedema-telangiectasia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011914",
            "name": "HLTS",
            "description": ""
        },
        {
            "id": "MIM:607823",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607823",
            "name": "Hypotrichosis-lymphedema-telangiectasia syndrome",
            "description": "Hypotrichosis-lymphedema-telangiectasia syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111361"
    ],
    "unlinked_id_list": []
}