{
    "disease_id": "DOID:0070146", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "familial dysautonomia, type 2"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "congenital insensitivity to pain-anhidrosis syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "CIPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "NTRK1 hereditary sensory and autonomic neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "neuropathy, congenital sensory, with anhidrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "insensitivity to pain, congenital, with anhidrosis; CIPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "HSAN IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "HSAN4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "hereditary sensory and autonomic neuropathy caused by mutation in NTRK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "HSNAN4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009746", 
            "name": "HSAN 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070146", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070146", 
            "name": "hereditary sensory neuropathy type IV"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070146", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070146", 
            "name": "insensitivity to pain, congenital, with anhidrosis"
        }, 
        {
            "url": "https://www.omim.org/entry/256800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:256800", 
            "name": "Congenital insensitivity to pain with anhidrosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070146", 
        "description": "A hereditary sensory neuropathy characterized by insensitivity to pain and anhidrosis that has_material_basis_in homozygous or compound heterozygous mutation in the NTRK1 gene on chromosome 1q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070146", 
        "name": "hereditary sensory neuropathy type 4"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/256800", 
            "id": "256800", 
            "database": "MIM"
        }
    ]
}
