Gene: LYZ ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.030 GeneticVariation disease BEFREE Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review. 28963698 2017
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.030 GeneticVariation disease BEFREE Lysozyme amyloidosis (ALys) is a rare form of hereditary amyloidosis that typically manifests with renal impairment, gastrointestinal (GI) symptoms, and sicca syndrome, whereas cardiac involvement is exceedingly rare and neuropathy has not been reported. 28049649 2017
Entrez Id: 4069
Gene Symbol: LYZ
LYZ 		0.030 GeneticVariation disease BEFREE We describe a new mutant lysozyme that presents with abdominal discomfort, diarrhea, weight loss, and sicca syndrome. 22978355 2012