{
    "disease_id": "DOID:0111730",
    "recommended_name": {
        "id": "DOID:0111730",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111730",
        "name": "familial episodic pain syndrome 2",
        "description": "A familial episodic pain syndrome characterized by adult-onset of paroxysmal pain mainly affecting the distal lower extremities that has_material_basis_in heterozygous mutation in the SCN10A gene on chromosome 3p22."
    },
    "synonyms": [
        {
            "id": "DOID:0111730",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111730",
            "name": "FEPS2",
            "description": ""
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "episodic pain syndrome, familial, 2",
            "description": "Any familial episodic pain syndrome in which the cause of the disease is a mutation in the SCN10A gene."
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "SCN10A familial episodic pain syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "episodic pain syndrome, familial, 2",
            "description": ""
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "episodic pain syndrome, familial, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "familial episodic pain syndrome caused by mutation in SCN10A",
            "description": ""
        },
        {
            "id": "MONDO:0014246",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014246",
            "name": "FEPS2",
            "description": ""
        },
        {
            "id": "MIM:615551",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615551",
            "name": "Episodic pain syndrome, familial, 2",
            "description": "Episodic pain syndrome, familial, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111730"
    ],
    "unlinked_id_list": []
}