Jansky–Bielschowsky disease
Jansky–Bielschowsky disease | |
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Classification and external resources | |
Specialty | endocrinology |
ICD-10 | E75.4 |
ICD-9-CM | 330.1 |
OMIM | 204500 |
DiseasesDB | 31535 |
MeSH | D009472 |
Jansky–Bielschowsky disease is a late-infantile form of neuronal ceroid lipofuscinosis associated with a deficiency in tripeptidyl peptidase I.[1]
Eponym
It is named for Jan Janský and Max Bielschowsky.[2]
References
External links
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