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CFH

complement factor H

gene with protein productOMIM: 1343707 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)5
Immunodeficiency with factor H anomalyORPHA:200421
→
Immunoglobulin-mediated membranoproliferative glomerulonephritisORPHA:329903
→
Familial drusenORPHA:75376
→
Atypical hemolytic uremic syndrome with complement gene abnormalityORPHA:544472
→
Dense deposit diseaseORPHA:93571
→
Ген-кандидат1
HELLP syndromeORPHA:244242
→
Биомаркер1
De novo thrombotic microangiopathy after kidney transplantationORPHA:244275
→
Данные: Orphadata (CC-BY-4.0)