{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "VAN DEN Ende-Gupta syndrome; VDEGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "Van den Ende Gupta syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "VDEGS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "blepharophimosis, arachnodactyly, and congenital contractures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "Marden-Walker-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "Marden Walker like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "Marden-Walker-like syndrome without psychomotor retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010959", 
            "name": "Marden Walker like syndrome without psychomotor retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111699", 
            "name": "blepharophimosis, arachnodactyly, and congenital contractures"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111699", 
            "name": "Marden-Walker-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111699", 
            "name": "VDEGS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111699", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111699", 
            "name": "Marden-Walker-like syndrome without psychmotor retardation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111699", 
        "description": "A syndrome characterized by severe contractual arachnodactyly, distinctive facial features, blepharophimosis, and absence of neurological involvement that has_material_basis_in homozygous or compound heterozygous mutation in SCARF2 on chromosome 22q11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111699", 
        "name": "Van den Ende-Gupta syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600920", 
            "id": "600920", 
            "database": "MIM"
        }
    ]
}