{
    "disease_id": "DOID:0111876", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "linear skin defects with multiple congenital anomalies type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "linear skin defects with cardiomyopathy and Other congenital anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "LSDMCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "linear skin defects with multiple congenital anomalies 3; LSDMCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010494", 
            "name": "NDUFB11 microphthalmia with linear skin defects syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111876", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111876", 
            "name": "LSDMCA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111876", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111876", 
            "name": "linear skin defects with cardiomyopathy and other congenital anomalies"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111876", 
        "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 NDUFB11 on chromosome Xp11.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111876", 
        "name": "linear skin defects with multiple congenital anomalies 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111876#disease-associations", 
            "id": "0111876", 
            "database": "Alliance of Genome Resources"
        }
    ]
}