{
    "disease_id": "DOID:0050548", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "neuropathy, hereditary sensory and autonomic, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "HSN 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "neuropathy, hereditary sensory, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "HSAN 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "hereditary sensory and autonomic neuropathy type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "hereditary sensory and autonomic neuropathy type 1 caused by mutation in SPTLC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "neuropathy, hereditary sensory and autonomic, type IA; HSAN1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "HSAN1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "hereditary sensory and autonomic neuropathy type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "SPTLC1 hereditary sensory and autonomic neuropathy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "neuropathy, hereditary sensory and autonomic, type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008086", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008086", 
            "name": "neuropathy, hereditary sensory radicular, autosomal dominant, type 1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050548", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050548", 
            "name": "familial dysautonomia, type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050548", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050548", 
            "name": "hereditary sensory and autonomic neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050548", 
        "description": "A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050548", 
        "name": "hereditary sensory neuropathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050548#disease-associations", 
            "id": "0050548", 
            "database": "Alliance of Genome Resources"
        }
    ]
}