Mondo Disease Ontology
6230 terms(s) returned
| Term Type: | Record: 4101 to 4150 of 6230 Records | Page: 83 of 125, First Previous Next Last | Show Records Per Page |
- ameloblastoma, non-human animal
- amelocerebrohypohidrotic syndrome
- amelogenesis
- amelogenesis imperfecta
- amelogenesis imperfecta hypomaturation type 2A2
- amelogenesis imperfecta hypomaturation type 2A3
- amelogenesis imperfecta hypomaturation type 2A4
- amelogenesis imperfecta hypomaturation type 2A5
- amelogenesis imperfecta type 1
- amelogenesis imperfecta type 1A
- amelogenesis imperfecta type 1B
- amelogenesis imperfecta type 1C
- amelogenesis imperfecta type 1E
- amelogenesis imperfecta type 1F
- amelogenesis imperfecta type 1G
- amelogenesis imperfecta type 1H
- amelogenesis imperfecta type 2
- amelogenesis imperfecta type 2A1
- amelogenesis imperfecta type 3B
- amelogenesis imperfecta, ACP4-related, dog
- amelogenesis imperfecta, ENAM-related, dog
- amelogenesis imperfecta, FAM83H-related, rabbit
- amelogenesis imperfecta, IIa 1K
- amelogenesis imperfecta, hypomaturation type, IIa6
- amelogenesis imperfecta, non-human animal
- amelogenesis imperfecta, type 1J
- amelogenesis imperfecta, type 3A
- amelogenesis imperfecta, type 3C
- ameloonychohypohidrotic syndrome
- amenorrhea
- amenorrhea-galactorrhea syndrome
- ametapodia, chicken
- ametapodia-1, chicken
- ametapodia-2, chicken
- ametropic amblyopia
- amide
- amidine-lyase activity
- amidinotransferase activity
- amine
- amine biosynthetic process
- amine metabolic process
- amine precursor uptake and decarboxylation cell
- amine transport
- amino acid
- amino acid activation
- amino acid binding
- amino acid biosynthetic process
- amino acid catabolic process
- amino acid metabolic process
- amino acid metabolism disease
