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
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal recessive limb-girdle muscular dystrophy type 2I
(6)
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)
Myopathy caused by variation in FKTN
(1)
Limb-girdle muscular dystrophy due to POMK deficiency
(0)
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)
Myopathy caused by variation in CRPPA
(0)
Myopathy caused by variation in GMPPB
(0)