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Results 1 - 8 of 8 for Cataract 6 multiple types
  1. PAX6 gene 
    ... 1; FVH1 KERATITIS, HEREDITARY OPTIC NERVE HYPOPLASIA, BILATERAL CATARACT 9, MULTIPLE TYPES; CTRCT9 PAIRED BOX GENE 6; PAX6 NCBI Gene ClinVar Azuma N, Yamaguchi Y, ...
    https://medlineplus.gov/genetics/gene/pax6 - Genetics
  2. Werner syndrome 
    ... aging early in life, such as cloudy lenses (cataracts) in both eyes, skin ... develop multiple, rare cancers during their lifetime. People with Werner ...
    https://medlineplus.gov/genetics/condition/werner-syndrome - Genetics
  3. TBC1D20 gene 
    ... DJ. Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind ... virus type 1 envelope proteins traffic toward virion assembly sites ...
    https://medlineplus.gov/genetics/gene/tbc1d20 - Genetics
  4. OPA3 gene 
    ... cell. A mutation that has been found in multiple people with autosomal dominant optic atrophy and cataract results in the production of a protein with ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  5. Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome 
    ... although the exact prevalence is unknown. At least six affected families have been described in ... one component of a protein called type IV collagen. Type IV collagen molecules attach to ...
    https://medlineplus.gov/...athy-aneurysms-and-muscle-cramps-syndrome - Genetics
  6. Isolated ectopia lentis 
    ... it is part of a syndrome that affects multiple parts of the body. Ectopia lentis is a common ... lentis is unknown. In Denmark, an estimated 6.4 per 100,000 individuals have ectopia lentis, ...
    https://medlineplus.gov/genetics/condition/isolated-ectopia-lentis - Genetics
  7. Mevalonate kinase deficiency 
    ... or clouding of the lens of the eye (cataracts). Affected adults may have short ... with multiple problems may live only into early childhood; mildly ...
    https://medlineplus.gov/.../condition/mevalonate-kinase-deficiency - Genetics
  8. Peters anomaly 
    ... and iris and mild to moderate corneal opacity. Type II is characterized by an incomplete separation of the ... Mutations in the FOXC1, ...
    https://medlineplus.gov/genetics/condition/peters-anomaly - Genetics