Progressive muscular dystrophy
MONDO:0016106Also known as: progressive muscular dystrophy
129 clinical trials for this condition and its sub-types, 2 tagged with Progressive muscular dystrophy itself.
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Sub-types of Progressive muscular dystrophy
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Myotonic dystrophy 56 trials · 57 incl. sub-types
8 sub-types
- Myotonic dystrophy type 1 45 trials Sub-types →
- Myotonic dystrophy type 2 11 trials
- Congenital myotonic dystrophy 9 trials
- Childhood-onset Steinert myotonic dystrophy 2 trials
- Juvenile-onset Steinert myotonic dystrophy 2 trials
- Adult-onset Steinert myotonic dystrophy 0 trials
- Late-onset Steinert myotonic dystrophy 0 trials
- Myotonic cataract 0 trials
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Facioscapulohumeral muscular dystrophy 36 trials · 40 incl. sub-types
5 sub-types
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Limb-girdle muscular dystrophy 17 trials · 26 incl. sub-types
3 sub-types
- Autosomal recessive limb-girdle muscular dystrophy 0 trials · 18 incl. sub-types Sub-types →
- Muscular dystrophy, limb-girdle, autosomal dominant 0 trials · 4 incl. sub-types Sub-types →
- POMGNT2-related limb-girdle muscular dystrophy R24 1 trial
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Oculopharyngeal muscular dystrophy 3 trials
2 sub-types
- Oculopharyngeal muscular dystrophy 1 0 trials
- Oculopharyngeal muscular dystrophy 2 0 trials
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Emery-Dreifuss muscular dystrophy 1 trial · 3 incl. sub-types
4 sub-types
- Autosomal dominant Emery-Dreifuss muscular dystrophy 0 trials · 3 incl. sub-types Sub-types →
- Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 trials
- X-linked Emery-Dreifuss muscular dystrophy 0 trials Sub-types →
- Scapuloperoneal myopathy 0 trials Sub-types →
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8 sub-types
- Tukel syndrome 0 trials
- Congenital fibrosis of extraocular muscles type 1 0 trials
- Fibrosis of extraocular muscles, congenital, 2 0 trials
- Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement 0 trials
- Fibrosis of extraocular muscles, congenital, 3b 0 trials
- Fibrosis of extraocular muscles, congenital, 3c 0 trials
- Fibrosis of extraocular muscles, congenital, 5 0 trials
- Fibrosis of extraocular muscles, congenital, with synergistic divergence 0 trials
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Bethlem myopathy 0 trials
4 sub-types
- Bethlem myopathy 1A 0 trials
- Bethlem myopathy 1B 0 trials
- Bethlem myopathy 1C 0 trials
- Bethlem myopathy 2 0 trials
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1 sub-type
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Oculopharyngodistal myopathy 0 trials
5 sub-types
- Oculopharyngodistal myopathy 1 0 trials
- Oculopharyngodistal myopathy 2 0 trials
- Oculopharyngodistal myopathy 3 0 trials
- Oculopharyngodistal myopathy 4 0 trials
- Oculopharyngodistal myopathy 5 0 trials
Most studied deeper sub-types
Autosomal recessive limb-girdle muscular dystrophy type 2I
(8)
Autosomal recessive limb-girdle muscular dystrophy type 2A
(5)
Autosomal recessive limb-girdle muscular dystrophy type 2E
(5)
Autosomal recessive limb-girdle muscular dystrophy type 2C
(4)
Autosomal recessive limb-girdle muscular dystrophy type 2B
(3)
Autosomal recessive limb-girdle muscular dystrophy type 2D
(3)
Emery-Dreifuss muscular dystrophy 2, autosomal dominant
(3)
Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)
(2)
Autosomal recessive limb-girdle muscular dystrophy type 2F
(2)
Autosomal recessive limb-girdle muscular dystrophy type 2L
(2)
Autosomal dominant limb-girdle muscular dystrophy type 1F
(1)
Autosomal dominant limb-girdle muscular dystrophy type 1G
(1)
Autosomal dominant limb-girdle muscular dystrophy type 1H
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2G
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2J
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2K
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2M
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2N
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2O
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2P
(1)