{
    "disease_id": "DOID:0111360", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019073", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019073", 
            "name": "glomerulonephritis with sparse hair and telangiectases"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019073", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019073", 
            "name": "HLTRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019073", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019073", 
            "name": "telangiectatic membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019073", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019073", 
            "name": "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome; HLTRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019073", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019073", 
            "name": "hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111360", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111360", 
            "name": "glomerulonephritis with sparse hair and telangiectases"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111360", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111360", 
            "name": "HLT-renal defect syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111360", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111360", 
            "name": "HLTRS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111360", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111360", 
            "name": "telangiectatic membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111360", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111360", 
            "name": "hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111360", 
        "description": "A syndrome characterized by onset in childhood of progressive hypotrichosis, lymphedema, telangiectasia, and renal defects that has_material_basis_in heterozygous mutation in SOX18 on chromosome 20q13.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111360", 
        "name": "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111360#disease-associations", 
            "id": "0111360", 
            "database": "Alliance of Genome Resources"
        }
    ]
}