{
    "disease_id": "DOID:0111876",
    "recommended_name": {
        "id": "DOID:0111876",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111876",
        "name": "linear skin defects with multiple congenital anomalies 3",
        "description": "A linear skin defects with multiple congenital anomalies characterized by linear skin defects, cardiomyopathy, and various other congenital anomalies that has_material_basis_in heterozygous mutation in the NDUFB11 gene on chromosome Xp11.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111876",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111876",
            "name": "LSDMCA3",
            "description": ""
        },
        {
            "id": "DOID:0111876",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111876",
            "name": "linear skin defects with cardiomyopathy and other congenital anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "linear skin defects with multiple congenital anomalies 3",
            "description": "Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the NDUFB11 gene."
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "NDUFB11 microphthalmia with linear skin defects syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "linear skin defects with multiple congenital anomalies 3",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "linear skin defects with multiple congenital anomalies 3, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "linear skin defects with multiple congenital anomalies type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11",
            "description": ""
        },
        {
            "id": "MONDO:0010494",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010494",
            "name": "LSDMCA3",
            "description": ""
        },
        {
            "id": "MIM:300952",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300952",
            "name": "Linear skin defects with multiple congenital anomalies 3",
            "description": "Linear skin defects with multiple congenital anomalies 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111876"
    ],
    "unlinked_id_list": []
}