Mondo Disease Ontology
2687 terms(s) returned
| Term Type: | Record: 2001 to 2050 of 2687 Records | Page: 41 of 54, First Previous Next Last | Show Records Per Page |
- neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor
- neuroepithelial neoplasm
- neuroepithelioma
- neurofaciodigitorenal syndrome
- neurofacioskeletal syndrome with or without renal agenesis
- neuroferritinopathy
- neurofibroma
- neurofibroma of gallbladder
- neurofibroma of spinal cord
- neurofibroma of the esophagus
- neurofibroma of the heart
- neurofibroma, non-human animal
- neurofibromatosis
- neurofibromatosis type 1
- neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
- neurofibromatosis, NF1-related, pig
- neurofibromatosis, cattle
- neurofibromatosis, familial spinal
- neurofibromatosis, non-human animal
- neurofibromatosis, teleost fishes
- neurofibromatosis, type III, mixed central and peripheral
- neurofibromatosis, type IV, of Riccardi
- neurofibromatosis-Noonan syndrome
- neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome
- neurofibrosarcoma
- neurofibrosarcoma, non-human animal
- neurogenesis
- neurogenic arthropathy
- neurogenic bowel
- neurogenic muscular atrophy, dog
- neurogenic muscular atrophy, non-human animal
- neurogenic myopathy, non-human animal
- neurogenic palpebral tumor
- neurogenic placode
- neurogenic scapuloperoneal syndrome, Kaeser type
- neurogenic thoracic outlet syndrome
- neurogenic urinary bladder dysfunction, non-human animal
- neurohypophyseal diabetes insipidus
- neurohypophysis
- neurohypophysis granular cell tumor
- neuroleptic malignant syndrome
- neurologic disease, infantile multisystem, with osseous fragility
- 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 muscular channelopathy due to a genetic calcium channel defect
- neurological muscular channelopathy due to a genetic chloride channel defect
- neurological muscular channelopathy due to a genetic potassium channel defect
- neurological muscular channelopathy due to a genetic sodium channel defect
- neurological pain disorder
