{
    "disease_id": "DOID:0110717", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "micro syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "RAB3GAP2 Warburg micro syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "WARBURG micro syndrome 2; WARBM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "WARBM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "Warburg micro syndrome caused by mutation in RAB3GAP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013641", 
            "name": "Warburg micro syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110717", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110717", 
            "name": "Micro Syndrome 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110717", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110717", 
            "name": "WARBM2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110717", 
        "description": "A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP2 gene on chromosome 1q41.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110717", 
        "name": "Warburg micro syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614225", 
            "id": "614225", 
            "database": "MIM"
        }
    ]
}