Mondo Disease Ontology
2360 terms(s) returned
| Term Type: | Record: 1751 to 1800 of 2360 Records | Page: 36 of 48, First Previous Next Last | Show Records Per Page |
- 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
- neurofibromatosis/schwannomatosis
- neurofibrosarcoma
- neurogenesis
- neurogenic arthropathy
- neurogenic bowel
- neurogenic muscular atrophy, dog
- neurogenic muscular atrophy, non-human animal
- neurogenic palpebral tumor
- neurogenic placode
- neurogenic scapuloperoneal syndrome, Kaeser type
- neurogenic thoracic outlet syndrome
- 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
- neurological syndrome, dog
- neurological syndrome, horse
- neurological syndrome, non-human animal
- neurolymphomatosis
- neuroma
- neuromere
- neurometabolic disorder due to serine deficiency
- neuromuscular channelopathy, KCNG1-related, cattle
- 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)
