{
    "disease_id": "DOID:0070155",
    "recommended_name": {
        "id": "DOID:0070155",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070155",
        "name": "hereditary sensory and autonomic neuropathy type 2A",
        "description": "A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has_material_basis_in homozygous or compound heterozygous mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070155",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070155",
            "name": "HSAN2A",
            "description": ""
        },
        {
            "id": "DOID:0070155",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070155",
            "name": "hereditary sensory and autonomic neuropathy type IIA",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "neuropathy, hereditary sensory and autonomic, type 2A",
            "description": "A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has material basis in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13"
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "HSAN 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "HSAN2A",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "HSN 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "neuropathy, hereditary sensory and autonomic, type II",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "neuropathy, hereditary sensory and autonomic, type IIA",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "neuropathy, hereditary sensory, type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024309",
            "name": "Morvan disease",
            "description": ""
        },
        {
            "id": "MIM:201300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/201300",
            "name": "Neuropathy, hereditary sensory and autonomic, 2A",
            "description": "Neuropathy, hereditary sensory and autonomic, 2A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070155"
    ],
    "unlinked_id_list": []
}