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 43376 - 43400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0015397 Disorder of eye CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C1510586 Autism Spectrum Disorders CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0235946 Cerebral atrophy CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0268689 Vitamin D-dependent rickets, type 1 CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0239946 Fibrosis, Liver CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0497327 Dementia CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0005684 Malignant neoplasm of urinary bladder CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0011991 Diarrhea CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0013595 Eczema CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0027051 Myocardial Infarction CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0153452 Malignant neoplasm of gallbladder CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0004096 Asthma CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C4721453 Peripheral Nervous System Diseases CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0028754 Obesity CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0151313 Sensory neuropathy CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0007222 Cardiovascular Diseases CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0027066 Myoclonus CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C1956346 Coronary Artery Disease CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0027765 nervous system disorder CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0393720 Reflex Epilepsy, Photosensitive CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C1621958 Glioblastoma Multiforme CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0010068 Coronary heart disease CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0242379 Malignant neoplasm of lung CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C3714756 Intellectual Disability CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0017638 Glioma BDH1 622 3-hydroxybutyrate dehydrogenase 1 Q02338

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024