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 62626 - 62650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0270914 Hereditary Motor and Sensory-Neuropathy Type II FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0270911 Charcot-Marie-Tooth Disease, Type Ia (disorder) FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C3203102 Idiopathic pulmonary arterial hypertension FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C1384666 hearing impairment FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0010417 Cryptorchidism FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0018817 Atrial Septal Defects FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0086543 Cataract FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0524851 Neurodegenerative Disorders FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0020255 Hydrocephalus FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0555198 Malignant Glioma FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0003467 Anxiety FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C1408174 Hypertrophic neuropathy of infancy FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C1862939 AMYOTROPHIC LATERAL SCLEROSIS 1 FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0020224 Polyhydramnios FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0031117 Peripheral Neuropathy FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0020545 Hypertension, Renovascular FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0017572 Gingival Recession FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0011581 Depressive disorder FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0000768 Congenital Abnormality FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0033860 Psoriasis FAM20B 9917 FAM20B glycosaminoglycan xylosylkinase O75063
C0013720 Ehlers-Danlos Syndrome FAM20B 9917 FAM20B glycosaminoglycan xylosylkinase O75063
C0432242 Desbuquois syndrome FAM20B 9917 FAM20B glycosaminoglycan xylosylkinase O75063
C0041696 Unipolar Depression LPGAT1 9926 lysophosphatidylglycerol acyltransferase 1 Q92604
C1269683 Major Depressive Disorder LPGAT1 9926 lysophosphatidylglycerol acyltransferase 1 Q92604
C0028754 Obesity LPGAT1 9926 lysophosphatidylglycerol acyltransferase 1 Q92604

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Last updated: August 19, 2024