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 60026 - 60050 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0027765 nervous system disorder PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0037773 Spastic Paraplegia, Hereditary PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0154681 Anterior Horn Cell Disease PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C1848745 Oliver-McFarlane syndrome PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0442874 Neuropathy PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0011882 Diabetic Neuropathies PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C3714756 Intellectual Disability PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0020758 Congenital ichthyosis PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0020757 Ichthyoses PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0271683 Polyneuropathy, Motor PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
C0917799 Hypersomnia PNPLA6 10908 patatin like phospholipase domain containing 6 Q8IY17
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

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Last updated: August 19, 2024