{
    "disease_id": "DOID:0110716",
    "recommended_name": {
        "id": "DOID:0110716",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110716",
        "name": "Warburg micro syndrome 1",
        "description": "A Warburg micro syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severely impaired intellectual development, spastic diplegia, and hypogonadism that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110716",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110716",
            "name": "Micro Syndrome 1",
            "description": ""
        },
        {
            "id": "DOID:0110716",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110716",
            "name": "WARBM1",
            "description": ""
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "Warburg micro syndrome 1",
            "description": "Any Warburg micro syndrome in which the cause of the disease is a mutation in the RAB3GAP1 gene."
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "RAB3GAP1 Warburg micro syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "WARBM1",
            "description": ""
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "Warburg micro syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "Warburg micro syndrome caused by mutation in RAB3GAP1",
            "description": ""
        },
        {
            "id": "MONDO:0010822",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010822",
            "name": "Warburg micro syndrome type 1",
            "description": ""
        },
        {
            "id": "MIM:600118",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600118",
            "name": "Warburg micro syndrome 1",
            "description": "Warburg micro syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110716"
    ],
    "unlinked_id_list": []
}