Contents

Search


Interactions

molecular events

Related

SMPD1 (sphingomyelin phosphodiesterase) gene mutation; Niemann-Pick Disease Interpretation

Specific

ectonucleotide pyrophosphatase/phosphodiesterase family member 7; E-NPP 7; NPP-7; alkaline sphingomyelin phosphodiesterase; intestinal alkaline sphingomyelinase; alk-smase (ENPP7) olipudase alfa-rpcp (Xenpozyme) sphingomyelin phosphodiesterase 2; lyso-platelet-activating factor-phospholipase C; lyso-PAF-PLC; neutral sphingomyelinase; sphingomyelinase-2; N-smase; nsmase (SMPD2) sphingomyelin phosphodiesterase 3; neutral sphingomyelinase 2; sphingomyelinase-3; nSMase2 (SMPD3) Sphingomyelin phosphodiesterase 4 (neutral sphingomyelinase 3, nSMase3, nSMase-3, SMPD4, KIAA1418) sphingomyelin phosphodiesterase; acid sphingomyelinase; sphingomyelinase-1; asmase (SMPD1, ASM)

General

lipase lysosomal hydrolase phosphodiesterase pro apoptotic protein