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 10201 - 10225 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0270763 Familial Motor Neuron Disease PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0009714 Hepatic Fibrosis, Congenital PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0085084 Motor Neuron Disease PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0011570 Mental Depression PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0037050 Sick Building Syndrome PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C1854520 SEBASTIAN SYNDROME PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0022735 Klinefelter Syndrome PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0085636 Photophobia PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0235991 Small for gestational age (disorder) PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0339537 Cone monochromatism PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0037772 Spastic Paraplegia PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0002736 Amyotrophic Lateral Sclerosis PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0030567 Parkinson Disease PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C1857941 Brooke-Spiegler syndrome PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0029124 Optic Atrophy PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0342384 Idiopathic hypogonadotropic hypogonadism PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0018916 Hemangioma PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C4721453 Peripheral Nervous System Diseases PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0854723 Retinal Dystrophies PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0751495 Seizures, Focal PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0751602 Hereditary Autosomal Dominant Spastic Paraplegia PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C1306459 Primary malignant neoplasm PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0014544 Epilepsy PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0020619 Hypogonadism PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0007758 Cerebellar Ataxia PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17

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