Muscular dystrophy-dystroglycanopathy
MONDO:0018276Also known as: CMD due to dystroglycanopathy, muscular dystrophy-dystroglycanopathy, congenital muscular dystrophy due to dystroglycanopathy
6 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Muscular dystrophy-dystroglycanopathy
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14 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 A, 7 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 A13 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 A9 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
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8 0 trials
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Muscular dystrophy-dystroglycanopathy, type C 0 trials · 1 incl. sub-types
9 sub-types
- Autosomal recessive limb-girdle muscular dystrophy type 2K 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2M 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2N 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2O 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2P 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2T 1 trial
- Autosomal recessive limb-girdle muscular dystrophy type 2U 1 trial
- Limb-girdle muscular dystrophy due to POMK deficiency 0 trials
- Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8 0 trials
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8 sub-types
- Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3 0 trials
- Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4 0 trials
- Muscular dystrophy-dystroglycanopathy type B5 0 trials
- Muscular dystrophy-dystroglycanopathy type B6 0 trials
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.