{
    "disease_id": "DOID:0070157",
    "recommended_name": {
        "id": "DOID:0070157",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070157",
        "name": "hereditary sensory and autonomic neuropathy type 1C",
        "description": "A hereditary sensory and autonomic neuropathy type 1 that has_material_basis_in heterozygous mutation in the SPTLC2 gene on chromosome 14q24."
    },
    "synonyms": [
        {
            "id": "DOID:0070157",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070157",
            "name": "HSAN1C",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070157",
            "name": "hereditary sensory and autonomic neuropathy type IC",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070157",
            "name": "HSN1C",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070157",
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            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070157",
            "name": "hereditary sensory neuropathy type IC",
            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013337",
            "name": "neuropathy, hereditary sensory and autonomic, type 1C",
            "description": "A hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24."
        },
        {
            "id": "MONDO:0013337",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013337",
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            "description": ""
        },
        {
            "id": "MONDO:0013337",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013337",
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            "description": ""
        },
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/613640",
            "name": "Neuropathy, hereditary sensory and autonomic, 1C",
            "description": "Neuropathy, hereditary sensory and autonomic, 1C"
        }
    ],
    "children": [],
    "id_list": [
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    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0070157",
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            "url": "https://disease-ontology.org/term/DOID:0070157",
            "categories": []
        },
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            "url": "https://monarchinitiative.org/disease/MONDO:0013337",
            "categories": []
        },
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            "url": "https://www.omim.org/entry/613640",
            "categories": []
        }
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                    "name": "SPTLC2",
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                    "name": "KIAA0526",
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                    "name": "l(2)35Dc",
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                    "id": "0070157",
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        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0070157"
}
