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 62601 - 62625 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0030360 Papillon-Lefevre Disease FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0265213 Distal arthrogryposis syndrome FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0678222 Breast Carcinoma FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0078982 Arhinencephaly FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0270922 Peripheral demyelinating neuropathy FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0205713 Roussy-Levy Syndrome (disorder) FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0018818 Ventricular Septal Defects FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0751036 Hereditary Motor and Sensory Neuropathy Type I FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0002736 Amyotrophic Lateral Sclerosis FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0014544 Epilepsy FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0015300 Exophthalmos FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0006142 Malignant neoplasm of breast FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0011303 Demyelinating Diseases FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0035067 Renal Artery Stenosis FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0878544 Cardiomyopathies FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0025958 Microcephaly FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0039685 Tetralogy of Fallot FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0848558 Hypospadias FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0011206 Delirium FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0015934 Fetal Growth Retardation FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C1408182 Hereditary motor and sensory neuropathy, types I-IV FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0085084 Motor Neuron Disease FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C1531647 Cerebral ventriculomegaly FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C2875300 Peroneal muscular atrophy (axonal type) (hypertrophic type) FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562
C0700095 Central neuroblastoma FIG4 9896 FIG4 phosphoinositide 5-phosphatase Q92562

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Last updated: August 19, 2024