Loterre: Patologías humanas: Recklinghausen's neurofibromatosis

disease > genetic disease > hereditary disease > Recklinghausen's neurofibromatosis

disease > skin appendages disease > skin disease > Recklinghausen's neurofibromatosis

disease > tumor > benign neoplasm > neurofibromatosis > Recklinghausen's neurofibromatosis

disease > nervous system diseases > neurofibromatosis > Recklinghausen's neurofibromatosis

disease > congenital disease > phacomatosis > neurofibromatosis > Recklinghausen's neurofibromatosis

Recklinghausen's neurofibromatosis

Neurofibromatosis type I (NF-1) is a complex multi-system human disorder caused by the mutation of a gene on chromosome 17 that is responsible for production of a protein called neurofibromin which is needed for normal function in many human cell types. (Wikipedia)

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