{
    "disease_id": "DOID:0070152",
    "recommended_name": {
        "id": "DOID:0070152",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070152",
        "name": "hereditary sensory and autonomic neuropathy type 1A",
        "description": "A hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has_material_basis_in heterozygous mutation in the SPTLC1 gene on chromosome 9q22."
    },
    "synonyms": [
        {
            "id": "DOID:0070152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070152",
            "name": "HSAN1A",
            "description": ""
        },
        {
            "id": "DOID:0070152",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070152",
            "name": "hereditary sensory and autonomic neuropathy type IA",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "neuropathy, hereditary sensory and autonomic, type 1A",
            "description": "An axonal form of hereditary motor and sensory neuropathy distinguished by prominent early sensory loss and later positive sensory phenomena, caused by mutations in SPTLC1."
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "HSAN1A",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "SPTLC1 hereditary sensory and autonomic neuropathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "hereditary sensory and autonomic neuropathy type 1 caused by mutation in SPTLC1",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "hereditary sensory and autonomic neuropathy type IA",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "HSAN 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "HSN 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "hereditary sensory and autonomic neuropathy type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "neuropathy, hereditary sensory and autonomic, type IA",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "neuropathy, hereditary sensory radicular, autosomal dominant, type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0008086",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008086",
            "name": "neuropathy, hereditary sensory, type 1A",
            "description": ""
        },
        {
            "id": "MIM:162400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/162400",
            "name": "Neuropathy, hereditary sensory and autonomic, 1A",
            "description": "Neuropathy, hereditary sensory and autonomic, 1A"
        }
    ]
}