{
    "disease_id": "DOID:0111343", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007537", 
            "name": "Lehman syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007537", 
            "name": "lateral meningocele syndrome; LMNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007537", 
            "name": "Lms"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007537", 
            "name": "LMNS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111343", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111343", 
            "name": "Lehman syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111343", 
        "description": "A syndrome characterized by facial anomalies, hyperextensibility, hypotonia, and meningocele-related neurologic dysfunction that has_material_basis_in heterozygous mutation in NOTCH3 on chromosome 19p13.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111343", 
        "name": "lateral meningocele syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/130720", 
            "id": "130720", 
            "database": "MIM"
        }
    ]
}