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 |
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