{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "Warburg micro syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "micro syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "WARBM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "Warburg micro syndrome caused by mutation in RAB3GAP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "WARBURG micro syndrome 1; WARBM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "micro syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "Warburg micro syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010822", 
            "name": "RAB3GAP1 Warburg micro syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060237", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060237", 
            "name": "WARBM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060237", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060237", 
            "name": "Warburg-Sjo-Fledelius syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060237", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060237", 
            "name": "micro syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/600118", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600118", 
            "name": "Warburg micro syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060237", 
        "description": "A syndrome characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060237", 
        "name": "Warburg micro syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600118", 
            "id": "600118", 
            "database": "MIM"
        }
    ]
}