dystrophy's Usage Examples:

Mutations are associated with Bietti"s crystalline dystrophy and retinitis pigmentosas.

trichothiodystrophy have photosensitivity, which divides the classification into syndromes with or without photosensitivity; BIDS and PBIDS, and IBIDS.

Those could be: dystrophy, myopathy and mitochondrial disorders.

Dystrophies (IC3D) renamed the condition "CHED1" to become posterior polymorphous corneal dystrophy, and renamed the condition "CHED2" to become, simply.

mutations in the dystrophin gene can cause different forms of muscular dystrophy, a disease characterized by progressive muscular wasting.

a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans".

ectrodactyly, and macular dystrophy; 225280; CDH3 Ectodermal dysplasia, hidrotic; 129500; GJB6 Ectodermal dysplasia, hypohidrotic, autosomal dominant; 129490;.

fatal cardiomyopathy, core myopathy with heart disease, centronuclear myopathy, limb-girdle muscular dystrophy type 2J, familial dilated cardiomyopathy 9.

studies in the Sir William Dunn School of Pathology, Oxford, taking post-doctoral research on the molecular basis of muscular dystrophy.

Meckel syndrome Megaloblastic anemia-1, Finnish and Norwegian type Mulibrey nanism Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies).

In June of the same year, Vertex announced it would acquire Exonics Therapeutics for up to "1 billion and collaborate with CRISPR Therapeutics, boosting its development of treatments for Duchenne muscular dystrophy and Myotonic Dystrophy Type 1.

children’s diseases, particularly respiratory disorders, dystrophy, and avitaminosis and child pathology.

Synonyms:

osteodystrophy, degenerative disorder,