{
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013142", 
            "name": "RETREG1 hereditary sensory and autonomic neuropathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013142", 
            "name": "neuropathy, hereditary sensory and autonomic, type IIB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013142", 
            "name": "hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013142", 
            "name": "HSAN2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013142", 
            "name": "hereditary sensory and autonomic neuropathy type IIB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070150", 
            "name": "hereditary sensory and autonomic neuropathy type IIB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070150", 
            "name": "HSAN2B"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613115", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070150", 
        "description": "A hereditary sensory and autonomic neuropathy type 2 characterized by early childhood onset of distal sensory impairment that has_material_basis_in homozygous mutation in the FAM134B gene on chromosome 5p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070150", 
        "name": "hereditary sensory and autonomic neuropathy type 2B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613115", 
            "id": "613115", 
            "database": "MIM"
        }
    ]
}