Experimental Factor Ontology
3015 terms(s) returned
| Term Type: | Record: 2201 to 2250 of 3015 Records | Page: 45 of 61, First Previous Next Last | Show Records Per Page |
- neuroligin-3 (human)
- neuroligin-3, signal peptide removed form (human)
- neuroligin-4, X-linked
- neuroligin-4, X-linked (human)
- neuroligin-4, X-linked, signal peptide removed form
- neuroligin-4, X-linked, signal peptide removed form (human)
- neuroligin-4, Y-linked
- neuroligin-4, Y-linked (human)
- neuroligin-4, Y-linked, signal peptide removed form (human)
- neuroligin-4, x-linked measurement
- neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
- neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
- neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2
- neurological pain disorder
- neuroma
- neuromast
- neuromedin U
- neuromedin-B
- neuromedin-B (human)
- neuromedin-B measurement
- neuromedin-B proteolytic cleavage product
- neuromedin-B, signal peptide removed form
- neuromedin-B, signal peptide removed form (human)
- neuromedin-S
- neuromedin-S (human)
- neuromedin-S proteolytic cleavage product
- neuromedin-U
- neuromedin-U (human)
- neuromedin-U proteolytic cleavage product
- neurometabolic disorder due to serine deficiency
- neuromodulin
- neuromodulin (human)
- neuromuscular disease
- neuromuscular disease and ocular or auditory anomalies with or without seizures
- neuromuscular disease caused by qualitative or quantitative defects of TRIM32
- neuromuscular disease caused by qualitative or quantitative defects of alpha-actin
- neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan
- neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)
- neuromuscular disease caused by qualitative or quantitative defects of dysferlin
- neuromuscular disease caused by qualitative or quantitative defects of dystrophin
- neuromuscular disease caused by qualitative or quantitative defects of myofibrillar proteins
- neuromuscular disease caused by qualitative or quantitative defects of nebulin
- neuromuscular disease caused by qualitative or quantitative defects of perlecan
- neuromuscular disease caused by qualitative or quantitative defects of plectin
- neuromuscular disease caused by qualitative or quantitative defects of protein SERCA1
- neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1
- neuromuscular disease caused by qualitative or quantitative defects of telethonin
- neuromuscular disease caused by qualitative or quantitative defects of titin
- neuromuscular disease caused by qualitative or quantitative defects of tropomyosin
- neuromuscular disease, congenital, with uniform type 1 fiber
