{
    "disease_id": "DOID:0111549", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "ALSG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "parotid aplasia or hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "congenital absence of lacrimal puncta and salivary glands"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "salivary glands, absence of, include"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "salivary glands, absence of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008397", 
            "name": "aplasia of lacrimal and salivary glands; ALSG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111549", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111549", 
            "name": "congenital absence of lacrimal puncta and salivary glands"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111549", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111549", 
            "name": "ALSG"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111549", 
        "description": "A syndrome characterized by irritable eyes, epiphora, xerostomia, variable aplasia or hypoplasia of the lacrimal, parotid, submandibular, and sublingual glands, and absence of the lacrimal puncta that has_material_basis_in heterozygous mutation in FGF10 on chromosome 5p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111549", 
        "name": "aplasia of lacrimal and salivary glands"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111549#disease-associations", 
            "id": "0111549", 
            "database": "Alliance of Genome Resources"
        }
    ]
}