|
fukuyama type cerebromuscular dystrophy
|
D058494 |
|
|
fukuyama type congenital muscular dystrophy
|
D058494 |
|
|
type a1 congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies
|
D058494 |
|
|
type a1 congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|
D058494 |
|
|
muscular dystrophy, congenital, fukuyama type
|
D058494 |
|
|
POMT1-Related muscle-eye-brain diseases
|
D058494 |
|
|
muscular dystrophy, limb-girdle, autosomal recessive, with mental retardation
|
D058494 |
|
|
POMT1-Related muscle-eye-brain disease
|
D058494 |
|
|
fukuyama muscular dystrophy
|
D058494 |
|
|
congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies, type a1
|
D058494 |
|
|
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type a1
|
D058494 |
|
|
muscular dystrophy due to defective glycosylation of dystroglycan 4a
|
D058494 |
|
|
walker-warburg syndrome, fktn-related
|
D058494 |
|
|
muscular dystrophy, fukuyama
|
D058494 |
|
|
cerebromuscular dystrophy, fukuyama type
|
D058494 |
|
