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Results 1 - 8 of 8 for Myopia "21," autosomal dominant
  1. Stickler syndrome 
    ... 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia. Eur J Hum Genet. 2019 Mar;27(3):369-377. doi: 10.1038/s41431-018-0316-y. Epub 2018 Dec 19. ... P, Snead MP. Autosomal Recessive Stickler Syndrome. Genes (Basel). 2022 Jun 24; ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  2. Myhre syndrome 
    ... syndrome. SMAD4 Myhre syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  3. Spondyloperipheral dysplasia 
    ... dysplasia. COL2A1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../condition/spondyloperipheral-dysplasia - Genetics
  4. Costello syndrome 
    ... symptoms. HRAS This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  5. Spondyloepiphyseal dysplasia congenita 
    ... COL2A1 Typically, SED congenita is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../spondyloepiphyseal-dysplasia-congenita - Genetics
  6. Bohring-Opitz syndrome 
    ... condition. ASXL1 Bohring-Opitz syndrome is considered an autosomal dominant condition, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/bohring-opitz-syndrome - Genetics
  7. Marfan syndrome 
    ... syndrome. FBN1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/marfan-syndrome - Genetics
  8. Color vision deficiency 
    ... yellow color vision defects are inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/color-vision-deficiency - Genetics