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 |
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DisGeNET | July 29, 2024 |
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