HUGO ID Detailed Result 7897


HUGO ID 7897
Symbol NPC1
Name Niemann-Pick disease, type C1
#Occurrence 6
#Paper 3

 


PMID Match String Actual String Score Flanking text Edited by Edit
15210305NPCNP-C0.3neurovisceral lipid storage disorder Niemann_amp_#x2013 Pick type C disease (NP-C) NP-C 84 
15210305NPCNP-C0.3NP-C is a neurodevelopmental disorder characterized by progressive neurodegeneration and lysosomal 
18414597NPC1NPC10.9Niemann-Pick disease C is due to mutations in either the NPC1 or NPC2 genes resulting in defective cholesterol transport and cholesterol 
18751914NPC1NPC10.9Niemann-Pick disease C is due to mutations in either the NPC1 or NPC2 genes resulting in defective cholesterol transport and cholesterol 
18414597niemann-pick diseaseniemann pick disease1.0niemann pick diseases a and b are due to acidic sphingomyelinase deficiency resulting in sphingomyelin accumulation while niemann pick disease c is due to mutations in either the npc1 or npc2 genes resulting in defective cholesterol transport and cholesterol accumulation.  
18751914niemann-pick diseaseniemann pick disease1.0niemann pick diseases a and b are due to acidic sphingomyelinase deficiency resulting in sphingomyelin accumulation while niemann pick disease c is due to mutations in either the npc1 or npc2 genes resulting in defective cholesterol transport and cholesterol accumulation.