D054819Level 8
Hexosaminidase B
**Definition:** A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
**Tree numbers:** - D08.811.277.450.483.180.875
**Synonyms:** - Hex B
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