Mondo Disease Ontology
2344 terms(s) returned
| Term Type: | Record: 1751 to 1800 of 2344 Records | Page: 36 of 47, First Previous Next Last | Show Records Per Page |
- 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)
- 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, non-human animal
- neuromuscular disorder, congenital, with dysmorphic facies
- neuromuscular junction
- neuromuscular junction disease
