Congenital muscular dystrophy
MONDO:0019950A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.
Also known as: CMD, MDC, congenital MD
14 clinical trials for this condition and its sub-types, 1 tagged with Congenital muscular dystrophy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Congenital muscular dystrophy
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Congenital myasthenic syndrome 10 2 trials
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Muscular dystrophy-dystroglycanopathy 0 trials · 1 incl. sub-types
7 sub-types
- Muscular dystrophy-dystroglycanopathy, type A 1 trial Sub-types →
- Muscular dystrophy-dystroglycanopathy, type C 0 trials · 1 incl. sub-types Sub-types →
- DPM3-congenital disorder of glycosylation 0 trials Sub-types →
- Congenital muscular dystrophy with intellectual disability 0 trials
- Congenital muscular dystrophy with intellectual disability and severe epilepsy 0 trials
- Muscle-eye-brain disease with bilateral multicystic leucodystrophy 0 trials
- Muscular dystrophy-dystroglycanopathy, type B 0 trials Sub-types →
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Rigid spine syndrome 0 trials · 1 incl. sub-types
1 sub-type
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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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4 sub-types
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1 sub-type
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Congenital muscular dystrophy 1B 0 trials
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Congenital myopathy, Paradas type 0 trials
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Muscle-eye-brain disease 0 trials
9 sub-types
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11 0 trials
Most studied deeper sub-types
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)
Autosomal recessive limb-girdle muscular dystrophy type 2T
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2U
(1)
Desmin-related myopathy with Mallory body-like inclusions
(0)
Limb-girdle muscular dystrophy due to POMK deficiency
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
(0)
Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
(0)
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
(0)
Muscular dystrophy-dystroglycanopathy type B5
(0)