Experimental Factor Ontology
3015 terms(s) returned
| Term Type: | Record: 2101 to 2150 of 3015 Records | Page: 43 of 61, First Previous Next Last | Show Records Per Page |
- neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
- neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus
- neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome
- neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
- neurodevelopmental measurement
- neurodevelopmental, jaw, eye, and digital syndrome
- neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
- neuroectoderm
- neuroectodermal melanolysosomal disease
- neuroectodermal-endocrine syndrome
- neuroendocrine carcinoma
- neuroendocrine cell
- neuroendocrine cell hyperplasia of infancy
- neuroendocrine convertase 1
- neuroendocrine convertase 1 (human)
- neuroendocrine convertase 1 measurement
- neuroendocrine convertase 2
- neuroendocrine convertase 2 (human)
- neuroendocrine disorder
- neuroendocrine gland
- neuroendocrine neoplasm
- neuroendocrine protein 7B2
- neuroendocrine protein 7B2 (human)
- neuroendocrine protein 7B2, signal peptide removed form
- neuroendocrine secretory protein 55 isoform Nesp55 (human)
- neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade
- neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor
- neuroepithelial cell-transforming gene 1 protein
- neuroepithelial cell-transforming gene 1 protein (human)
- neuroepithelial cell-transforming gene 1 protein measurement
- neuroepithelial neoplasm
- neurofaciodigitorenal syndrome
- neurofacioskeletal syndrome with or without renal agenesis
- neurofascin
- neurofascin (human)
- neurofascin measurement
- neurofascin, signal peptide removed form (human)
- neuroferritinopathy
- neurofibrillary tangles measurement
- neurofibroma
- neurofibroma of gallbladder
- neurofibroma of spinal cord
- neurofibroma of the esophagus
- neurofibroma of the heart
- neurofibromatosis
- neurofibromatosis type 1
- neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
- neurofibromatosis, familial spinal
- neurofibromatosis-Noonan syndrome
- neurofibrosarcoma
