{
    "disease_id": "DOID:0111537", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "PEPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "rectal pain, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "submandibular, ocular, and rectal pain with flushing"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "pain, submandibular, ocular, and rectal, with flushing"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "Pexpd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "familial rectal pain"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008179", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008179", 
            "name": "familial rectal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111537", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111537", 
            "name": "submandibular, ocular and rectal pain with flushing"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111537", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111537", 
            "name": "PEPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111537", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111537", 
            "name": "PEXPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111537", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111537", 
            "name": "familial rectal pain"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111537", 
        "description": "An autonomic nervous system disease characterized by onset in the neonatal period or infancy of paroxysms of rectal, ocular, or submandibular pain with flushing that has_material_basis_in heterozygous mutation in SCN9A on chromosome 2q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111537", 
        "name": "paroxysmal extreme pain disorder"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111537#disease-associations", 
            "id": "0111537", 
            "database": "Alliance of Genome Resources"
        }
    ]
}