Mondo Disease Ontology
1617 terms(s) returned
| Term Type: | Record: 851 to 900 of 1617 Records | Page: 18 of 33, First Previous Next Last | Show Records Per Page |
- familial visceral amyloidosis
- familial visceral myopathy
- famililal cerebral cavernous malformations
- fanconi anemia, complementation group 10
- farmer's lung disease
- fascia
- fascia of Scarpa
- fascia of tail
- fascial dystrophy, congenital
- fasciculus of brain
- fasciculus of spinal cord
- fasciitis
- fascioliasis
- fascioloidiasis
- fasciolopsiasis
- fasting unconjugated hyperbilirubinemia, Bolivian squirrel monkey
- fat cell differentiation
- fat necrosis of breast
- fat pad
- fat-soluble vitamin (role)
- fat-soluble vitamin biosynthetic process
- fatal familial insomnia
- fatal infantile encephalocardiomyopathy
- fatal infantile hypertonic myofibrillar myopathy
- fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
- fatal multiple mitochondrial dysfunctions syndrome
- fatal post-viral neurodegenerative disorder
- fatty acid
- fatty acid anion
- fatty acid anion 3:0
- fatty acid biosynthetic process
- fatty acid derivative biosynthetic process
- fatty acid derivative catabolic process
- fatty acid derivative metabolic process
- fatty acid hydroxylase-associated neurodegeneration
- fatty acid metabolic process
- fatty acid oxidation
- fatty acyl-CoA reductase 1 deficiency
- fatty acyl-CoA reductase 1 upregulation
- fatty acyl-CoA reductase defects
- fatty liver disease
- fatty liver disease, nonalcoholic, susceptibility to, 2
- faucial diphtheria
- favism
- fear/anxiety related behavior
- feature_attribute
- febrile infection-related epilepsy syndrome
- febrile seizures, familial
- febrile seizures, familial, 1
- febrile seizures, familial, 10
