APP - Amyloid beta (A4) precursor protein (peptidase nexin-II, Alzheimer disease)
|
|
Diseases list
- Disease-causing germline mutation(s) in Early-onset autosomal dominant Alzheimer disease
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Arctic type
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Dutch type
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Flemish type
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Iowa type
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Italian type
- Disease-causing germline mutation(s) in Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Assessed
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
