Toxic Process Ontology
459 terms(s) returned
| Term Type: | Record: 351 to 400 of 459 Records | Page: 8 of 10, First Previous Next Last | Show Records Per Page |
- sphingomyelin accumulation in lysosome
- sphingomyelin accumulation in lysosome [Phospholipidosis - sphingomyelin disorder ]
- sphingomyelin accumulation in lysosome [Phospholipidosis - genetic- sphingomyelin disorder]
- sphingomyelin accumulation in lysosome of nervous system
- sphingomyelin accumulation in lysosome of nervous system [Niemann Pick Disease Type A (severe) ]
- sphingomyelin biosynthetic process
- sphingomyelin biosynthetic process[Niemann Pick Disease Type A]
- sphingomyelin biosynthetic process[Niemann Pick Disease Type B]
- sphingomyelin catabolic process
- sphingomyelin disorder (genetic)
- sphingomyelin disorder (phospholipidosis)
- sphingomyelin homeostasis imbalance [Niemann Pick Disease Type A/ B]
- sphingomyelin homeostasis imbalance [Niemann Pick Disease Type A]
- sphingomyelin homeostasis imbalance [Niemann Pick Disease Type B]
- sphingomyelin homeostasis imbalance [Phospholipidosis - genetic]
- sphingomyelin homeostasis imbalance [Phospholipidosis - sphingomyelin disorder]
- sphingomyelin metabolic process
- sphingomyelin metabolism imbalance
- sphingomyelin metabolism imbalance [Niemann Pick Disease Type A/ B]
- sphingomyelin metabolism imbalance [Niemann Pick Disease Type A]
- sphingomyelin metabolism imbalance [Niemann Pick Disease Type B]
- sphingomyelin metabolism imbalance [Phospholipidosis - genetic- sphingomyelin disorder ]
- sphingomyelin metabolism imbalance [Phospholipidosis - sphingomyelin disorder]
- sphingomyelin metabolism imbalance [Phospholipidosis ]
- sphingomyelin metabolism imbalance in nervous system [Niemann Pick Disease Type A]
- sphingomyelin phosphodiesterase
- sphingomyelin phosphodiesterase inhibitor role
- sphingomyelinase gene mutation
- sphingomyelinase gene mutation [Niemann Pick Disease Type A/ B]
- sphingomyelinase gene mutation [Niemann Pick Disease Type A]
- sphingomyelinase gene mutation [Niemann Pick Disease Type B]
- sphingomyelinase gene mutation [Phospholipidosis - genetic- sphingomyelin disorder ]
- sphingophopholipid metabolism imbalance
- sphingophospholipid accumulation in lysosome
- sphingophospholipid catabolic process
- sphingosine
- sphingosine-1-phosphate
- spinal cord
- spleen
- spleen hyperfunction
- spleen hyperfunction [hepatic blood circulatory disorder]
- spleen malfunction
- spleen malfunction [Niemann Pick Disease Type A/ B]
- splenohepatomegaly
- splenohepatomegaly [Niemann Pick Disease Type A]
- splenohepatomegaly [Niemann Pick Disease Type B]
- splitting
- stabilizing lysosomal membrane structure
- stabilizing lysosomal membrane structure [Phospholipidosis]
- stabilizing membrane structure
