{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "insensitivity to pain, congenital, with gastrointestinal dysfunction and hyperhidrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "HSAN7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "CIP with hyperhidrosis and gastrointestinal dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "HSAN with hyperhidrosis and gastrointestinal dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "SCN11A autosomal dominant hereditary sensory and autonomic neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "neuropathy, hereditary sensory and autonomic, type VII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "neuropathy, hereditary sensory and autonomic, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "neuropathy, hereditary sensory and autonomic, type VII; HSAN7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "HSAN VII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "hereditary sensory and autonomic neuropathy type VII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "HSAN 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014244", 
            "name": "autosomal dominant hereditary sensory and autonomic neuropathy caused by mutation in SCN11A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070149", 
            "name": "hereditary sensory and autonomic neuropathy type VII"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070149", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070149", 
            "name": "HSAN7"
        }, 
        {
            "url": "https://www.omim.org/entry/615548", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615548", 
            "name": "Neuropathy, hereditary sensory and autonomic, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070149", 
        "description": "A hereditary sensory neuropathy characterized by insensitivity to pain, mild muscle weakness, delayed motor development, hyperhidrosis and gastrointestinal dysfunction that has_material_basis_in heterozygous mutation in the SCN11A gene on chromosome 3p22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070149", 
        "name": "hereditary sensory and autonomic neuropathy type 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615548", 
            "id": "615548", 
            "database": "MIM"
        }
    ]
}
