|
congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies, type a1
|
D058494 |
|
|
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type a1
|
D058494 |
|
|
POMT1-Related muscle-eye-brain disease
|
D058494 |
|
|
muscular dystrophy due to defective glycosylation of dystroglycan 4a
|
D058494 |
|
|
muscular dystrophy, fukuyama
|
D058494 |
|
|
cerebromuscular dystrophy, fukuyama type
|
D058494 |
|
|
POMT1 related muscle eye brain disease
|
D058494 |
|
|
aplastic anemia, idiopathic
|
C538494 |
|
|
muscular dystrophy, limb-girdle, autosomal recessive, with mental retardation
|
D058494 |
|
|
muscular dystrophy, limb-girdle, type 2k
|
D058494 |
|
|
disease, POMT1-Related muscle-eye-brain
|
D058494 |
|
|
dystrophy, fukuyama muscular
|
D058494 |
|
|
fukuyama congenital muscular dystrophy
|
D058494 |
|
|
limb-girdle, autosomal recessive, with mental retardation muscular dystrophy
|
D058494 |
|
|
walker warburg syndrome, fktn related
|
D058494 |
|
