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 2876 - 2900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0205645 Adenocarcinoma, Tubular PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0005695 Bladder Neoplasm PLCE1 51196 phospholipase C epsilon 1 Q9P212
C1708349 Hereditary Diffuse Gastric Cancer PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0751688 Malignant Squamous Cell Neoplasm PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0265219 Miller Dieker syndrome PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0153452 Malignant neoplasm of gallbladder PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0017154 Gastritis, Atrophic PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0343641 Human papilloma virus infection PLCE1 51196 phospholipase C epsilon 1 Q9P212
C0006826 Malignant Neoplasms CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0042769 Virus Diseases CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0000768 Congenital Abnormality CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0027651 Neoplasms CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0699791 Stomach Carcinoma CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0014116 Endocardial Cushion Defects CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0019061 Hemolytic-Uremic Syndrome CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0272286 Thrombocytopenia due to platelet alloimmunization CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0039585 Androgen-Insensitivity Syndrome CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C2239176 Liver carcinoma CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C1306459 Primary malignant neoplasm CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0010054 Coronary Arteriosclerosis CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0023895 Liver diseases CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0011847 Diabetes CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0948008 Ischemic stroke CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0018939 Hematological Disease CLEC1B 51266 C-type lectin domain family 1 member B Q9P126
C0011849 Diabetes Mellitus CLEC1B 51266 C-type lectin domain family 1 member B Q9P126

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Last updated: August 19, 2024