Muscular dystrophy-dystroglycanopathy
MONDO:0018276Also known as: CMD due to dystroglycanopathy, muscular dystrophy-dystroglycanopathy, congenital muscular dystrophy due to dystroglycanopathy
40 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 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)
Muscular dystrophy-dystroglycanopathy, type A
(1)
Congenital muscular dystrophy with intellectual disability
(0)
Congenital muscular dystrophy with intellectual disability and severe epilepsy
(0)
DPM3-congenital disorder of glycosylation
(0)
Limb-girdle muscular dystrophy due to POMK deficiency
(0)
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
(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 A14
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
(0)