{
    "disease_id": "DOID:0111253", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008078", 
            "name": "neurofibromatosis, familial spinal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008078", 
            "name": "Fsnf"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "FSNF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "NF1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "Peripheral Neurofibromatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "familial spinal neurofibromatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "neurofibromatosis type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111253", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111253", 
            "name": "von Recklinghausen Disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111253", 
        "description": "A neurofibromatosis classically characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin or in some cases by a high load of spinal tumors that has_material_basis_in heterozygous mutation in NF1 on 17q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111253", 
        "name": "neurofibromatosis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111253#disease-associations", 
            "id": "0111253", 
            "database": "Alliance of Genome Resources"
        }
    ]
}