Searched for "Cataract".
98
results
found
on Genetics Home Reference.
Showing results 1 to 20.
- hypomyelination and congenital cataract condition summary
Found: Hypomyelination and congenital cataract is an inherited condition that...
- Rothmund-Thomson Syndrome condition summary
Found in name or synonym: Poikiloderma atrophicans and cataract
- hyperferritinemia-cataract syndrome condition summary
Found: Hyperferritinemia-cataract syndrome is a disorder characterized...
- congenital cataracts, facial dysmorphism, and neuropathy condition summary
Found in link title: Cataract
- oculofaciocardiodental syndrome condition summary
Found: ...include clouding of the lens (cataract) and a higher risk of glaucoma,...
- cataract definition
- MYH9-related disorder condition summary
Found in link title: Cataract
- FAM126A gene summary
Official name: family with sequence similarity 126, member A
Found: ...hypomyelination and congenital cataract. Most mutations delete a large...
- rhizomelic chondrodysplasia punctata condition summary
Found in link title: Congenital Cataract
- Wagner syndrome condition summary
Found: ...of the lens of the eye (cataract). A condition called erosive vitreoretinopathy...
- Chanarin-Dorfman syndrome condition summary
Found in link title: Cataract
- Werner syndrome condition summary
Found in link title: Cataract
- 1q21.1 microdeletion condition summary
Found in link title: Cataract
- microphthalmia condition summary
Found: ...of the lens of the eye (cataract) and a narrowed opening of the...
- coloboma condition summary
Found: ...of the lens of the eye (cataract), increased pressure inside the...
- Marinesco-Sjögren syndrome condition summary
Found in link title: Congenital cataract
- Lowe syndrome condition summary
Found in link title: Congenital Cataract
- FTL gene summary
Official name: ferritin, light polypeptide
Found: ...people with hyperferritinemia-cataract syndrome. Individuals affected...
- galactosemia condition summary
Found: ...of the lens of the eye (cataract), speech difficulties, and intellectual...
- OPA3 gene summary
Official name: optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Found: ...dominant optic atrophy and cataract (ADOAC). Autosomal dominant inheritance...
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