{
    "disease_id": "DOID:0050548",
    "recommended_name": {
        "id": "DOID:0050548",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050548",
        "name": "hereditary sensory neuropathy",
        "description": "A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages."
    },
    "synonyms": [
        {
            "id": "DOID:0050548",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050548",
            "name": "familial dysautonomia, type II",
            "description": ""
        },
        {
            "id": "DOID:0050548",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050548",
            "name": "hereditary sensory and autonomic neuropathy",
            "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"
        }
    ],
    "children": [
        {
            "id": "DOID:0070149",
            "label": "hereditary sensory and autonomic neuropathy type 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070161",
            "label": "hereditary sensory and autonomic neuropathy type 2",
            "link_status": false,
            "children": [
                {
                    "id": "DOID:0070155",
                    "label": "hereditary sensory and autonomic neuropathy type 2A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070150",
                    "label": "hereditary sensory and autonomic neuropathy type 2B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070147",
                    "label": "hereditary sensory neuropathy type 2C",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0070162",
            "label": "hereditary sensory and autonomic neuropathy type 1",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0070152",
                    "label": "hereditary sensory and autonomic neuropathy type 1A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070154",
                    "label": "hereditary sensory neuropathy type 1F",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070156",
                    "label": "hereditary sensory neuropathy type 1D",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070157",
                    "label": "hereditary sensory and autonomic neuropathy type 1C",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:11589",
            "label": "Riley-Day syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070158",
            "label": "hereditary sensory neuropathy type 1E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070151",
            "label": "hereditary sensory and autonomic neuropathy type 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070153",
            "label": "hereditary sensory and autonomic neuropathy type 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070146",
            "label": "hereditary sensory neuropathy type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070145",
            "label": "hereditary sensory and autonomic neuropathy type 5",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070158",
        "DOID:0050548",
        "DOID:0070145",
        "DOID:0070156",
        "DOID:0070155",
        "DOID:0070151",
        "DOID:0070162",
        "DOID:0070147",
        "DOID:0070146",
        "DOID:0070149",
        "DOID:0070157",
        "DOID:0070153",
        "DOID:0070152",
        "DOID:11589",
        "DOID:0070161",
        "DOID:0070154",
        "DOID:0070150"
    ],
    "unlinked_id_list": [
        "DOID:0070161"
    ]
}