Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan
MONDO:0018282Also known as: alpha-dystroglycanopathy, dystroglycanopathy, qualitative or quantitative defects of alpha-dystroglycan
8 clinical trials for this condition and its sub-types, 0 tagged with Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan
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Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types
9 sub-types
- Qualitative or quantitative defects of FKRP 0 trials · 8 incl. sub-types Sub-types →
- Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
- Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
- Qualitative or quantitative defects of protein O-mannosyltransferase 1 0 trials · 1 incl. sub-types Sub-types →
- Qualitative or quantitative defects of protein O-mannosyltransferase 2 0 trials · 1 incl. sub-types Sub-types →
- Limb-girdle muscular dystrophy due to POMK deficiency 0 trials
Most studied deeper sub-types
Autosomal recessive limb-girdle muscular dystrophy type 2I
(8)
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 2T
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2U
(1)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
(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 without intellectual disability), type B4
(0)
Including sub-types (8)
Tagged with Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan (0)
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