Experimental Factor Ontology
4252 terms(s) returned
| Term Type: | Record: 3851 to 3900 of 4252 Records | Page: 78 of 86, First Previous Next Last | Show Records Per Page |
- 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
- muscular dystrophy, limb-girdle, autosomal dominant 4
- muscular dystrophy, limb-girdle, autosomal recessive 23
- muscular dystrophy, limb-girdle, autosomal recessive 26
- muscular dystrophy, limb-girdle, autosomal recessive 27
- muscular dystrophy, limb-girdle, autosomal recessive 28
- muscular dystrophy, limb-girdle, autosomal recessive 29
- muscular dystrophy-dystroglycanopathy
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
- muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
