DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 41851 - 41875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0021390 Inflammatory Bowel Diseases LYZ 4069 lysozyme P61626
C0031256 Petechiae LYZ 4069 lysozyme P61626
C0024894 Mastitis LYZ 4069 lysozyme P61626
C3887494 ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE LYZ 4069 lysozyme P61626
C1527336 Sjogren's Syndrome LYZ 4069 lysozyme P61626
C0002726 Amyloidosis LYZ 4069 lysozyme P61626
C0238198 Gastrointestinal Stromal Tumors LYZ 4069 lysozyme P61626
C0678222 Breast Carcinoma LYZ 4069 lysozyme P61626
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME LYZ 4069 lysozyme P61626
C0267380 Crohn's disease of the ileum LYZ 4069 lysozyme P61626
C0010606 Adenoid Cystic Carcinoma LYZ 4069 lysozyme P61626
C0699791 Stomach Carcinoma LYZ 4069 lysozyme P61626
C0011849 Diabetes Mellitus LYZ 4069 lysozyme P61626
C0041912 Upper Respiratory Infections LYZ 4069 lysozyme P61626
C0524620 Metabolic Syndrome X LYZ 4069 lysozyme P61626
C0020538 Hypertensive disease LYZ 4069 lysozyme P61626
C3888065 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT LYZ 4069 lysozyme P61626
C0027726 Nephrotic Syndrome LYZ 4069 lysozyme P61626
C0002395 Alzheimer's Disease LYZ 4069 lysozyme P61626
C0024623 Malignant neoplasm of stomach LYZ 4069 lysozyme P61626
C0022354 Jaundice, Obstructive LYZ 4069 lysozyme P61626
C0020877 Ileitis LYZ 4069 lysozyme P61626
C0031117 Peripheral Neuropathy LYZ 4069 lysozyme P61626
C0149516 Chronic sinusitis LYZ 4069 lysozyme P61626
C0442874 Neuropathy LYZ 4069 lysozyme P61626

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Last updated: August 19, 2024