{
    "disease_id": "DOID:0070145", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "HSAN V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "neuropathy, hereditary sensory and autonomic, type V; HSAN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "neuropathy, hereditary sensory and autonomic, type V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "NGF autosomal recessive hereditary sensory and autonomic neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "HSAN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "HSAN 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "congenital insensitivity to pain and thermal analgesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "insensitivity to pain, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "hereditary sensory and autonomic neuropathy type V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012092", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012092", 
            "name": "neuropathy, hereditary sensory and autonomic, type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070145", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070145", 
            "name": "HSAN5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070145", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070145", 
            "name": "hereditary sensory and autonomic neuropathy type V"
        }, 
        {
            "url": "https://www.omim.org/entry/608654", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608654", 
            "name": "Neuropathy, hereditary sensory and autonomic, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070145", 
        "description": "A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070145", 
        "name": "hereditary sensory and autonomic neuropathy type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608654", 
            "id": "608654", 
            "database": "MIM"
        }
    ]
}