{
    "disease_id": "DOID:0070151",
    "recommended_name": {
        "id": "DOID:0070151",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070151",
        "name": "hereditary sensory and autonomic neuropathy type 6",
        "description": "A hereditary sensory and autonomic neuropathy characterized by neonatal hypotonia, respiratory and feeding difficulties, impaired psychomotor development, and autonomic abnormalities that has_material_basis_in homozygous or compound heterozygous in the DST gene on chromosome 6p12."
    },
    "synonyms": [
        {
            "id": "DOID:0070151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070151",
            "name": "HSAN6",
            "description": ""
        },
        {
            "id": "DOID:0070151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070151",
            "name": "hereditary sensory and autonomic neuropathy type VI",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "hereditary sensory and autonomic neuropathy type 6",
            "description": "Any hereditary sensory and autonomic neuropathy in which the cause of the disease is a mutation in the DST gene."
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "DST hereditary sensory and autonomic neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "HSAN6",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "familial dysautonomia with contractures",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "hereditary sensory and autonomic neuropathy caused by mutation in DST",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "hereditary sensory and autonomic neuropathy type VI",
            "description": ""
        },
        {
            "id": "MONDO:0013839",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013839",
            "name": "neuropathy, hereditary sensory and autonomic, type VI",
            "description": ""
        },
        {
            "id": "MIM:614653",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614653",
            "name": "Neuropathy, hereditary sensory and autonomic, 6",
            "description": "Neuropathy, hereditary sensory and autonomic, 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070151"
    ],
    "unlinked_id_list": []
}