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 1851 - 1875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0026946 Mycoses CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C3714636 Pneumonitis CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0006826 Malignant Neoplasms CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0004153 Atherosclerosis CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0041296 Tuberculosis CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0003873 Rheumatoid Arthritis CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C1535939 Pneumocystis jiroveci pneumonia CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0027051 Myocardial Infarction CLEC6A 93978 C-type lectin domain containing 6A Q6EIG7
C0029456 Osteoporosis HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0020757 Ichthyoses HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0162809 Kallmann Syndrome HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0242350 Erectile dysfunction HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0016202 Flatfoot HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0029422 Osteochondrodysplasias HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0011847 Diabetes HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0342384 Idiopathic hypogonadotropic hypogonadism HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C1800706 Idiopathic Pulmonary Fibrosis HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0271623 Hypogonadotropic hypogonadism HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0036341 Schizophrenia HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0018418 Gynecomastia HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0009398 Color vision defect HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0010417 Cryptorchidism HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0036572 Seizures HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C0028754 Obesity HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243
C1609433 Congenital absence of kidneys syndrome HS6ST1 9394 heparan sulfate 6-O-sulfotransferase 1 O60243

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Last updated: August 19, 2024