Disease
Leptospirosis;Weil Disease
[ DI0002588 ]
- Summary
- A primary bacterial infectious disease that involves systemic infection, has material basis in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has sympto;Leptospirosis, also known as weil disease, is related to dengue disease and acute kidney failure. An important gene associated with Leptospirosis is PIK3C2A (Phosphatidylinositol-4-Phosphate 3-Kinase Catalytic Subunit Type 2 Alpha), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Emtricitabine and Doxycycline have been mentioned in the context of this disorder. Affiliated tissues include testes, kidney and liver, and relatedphenotypes are fever and arthralgia
- Synonym
- Disease, Weil Disease, Weil's FIEDLER DISEASE Fort Bragg fever H Haemorrhagic leptospiral jaundice Haemorrhagic leptospirosis with jaundice Haemorrhagic spirochaetal jaundice Hemorrhagic leptospiral jaundice Hemorrhagic leptospiral or spirochetal jaundice
- Xref
- CHV: 0000013134 CSP: 0368-3335 DO: DOID:2297 DXP: NOCODE DXP: U001041 ICD10: A27.0 ICD10AM: A27.0 ICD10CM: A27.0 ICD9CM: 100.0 LCH: U005015 LCH_NW: sh85145979 MDR: 10019014 MDR: 10024239 MDR: 10024240 MDR: 10047903 MDR: 10055283 MEDCIN: 31068 MEDCIN: 359957 MSH: D014895
Classification
| PMappKB GV ID | Genomic Location | Alt | ProAlt | Gene symbol | Relation |
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