Experimental Factor Ontology
4222 terms(s) returned
| Term Type: | Record: 3801 to 3850 of 4222 Records | Page: 77 of 85, First Previous Next Last | Show Records Per Page |
- multiple synostoses syndrome 4
- multiple system atrophy
- multiple system atrophy 1, susceptibility to
- multiple system atrophy, cerebellar type
- multisite chronic pain
- multisystem inflammatory syndrome in children and adults
- multisystemic smooth muscle dysfunction syndrome
- multivesicular body subunit 12B
- multivesicular body subunit 12B (human)
- mumps infectious disease
- mural granulosa cell
- murine neuroblastoma cholinergic cell line
- muscarinic acetylcholine receptor M1
- muscarinic antagonist
- muscle atrophy
- muscle cancer
- muscle cell
- muscle cell derived cell line
- muscle cell morphology trait
- muscle cramp
- muscle measurement
- muscle of pes
- muscle strain
- muscle structure
- muscle system process
- muscle tissue
- muscle tissue disorder
- muscle, skeletal receptor tyrosine-protein kinase
- muscle, skeletal receptor tyrosine-protein kinase (human)
- muscle, skeletal receptor tyrosine-protein kinase measurement
- muscle, skeletal receptor tyrosine-protein kinase, signal peptide removed form (human)
- muscle-eye-brain disease
- muscle-eye-brain disease with bilateral multicystic leucodystrophy
- muscleblind-like protein 1
- muscleblind-like protein 1 (human)
- muscleblind-like protein 2
- muscleblind-like protein 2 (human)
- muscular LMNA-interacting protein
- muscular LMNA-interacting protein (human)
- muscular atrophy
- muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
- muscular channelopathy
- muscular disease
- muscular dystrophy
- muscular dystrophy, adult-onset, with leukoencephalopathy
- muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
- muscular dystrophy, congenital, with cataracts and intellectual disability
- muscular dystrophy, congenital, with or without seizures
- muscular dystrophy, congenital, with rapid progression
- muscular dystrophy, limb-girdle, autosomal dominant
