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Results 1 - 7 of 7 for Myopia "19," autosomal dominant
  1. ... AUTOSOMAL DOMINANT; MYP15 MYOPIA 20, AUTOSOMAL DOMINANT; MYP20 MYOPIA 19, AUTOSOMAL DOMINANT; MYP19 PubMed Cheng CY, Schache M, Ikram MK, ...
  2. ... 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. Citation on PubMed Nixon TRW, Richards AJ, Martin ...
  3. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
  4. ... TUBA1A gene, the condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... of migration disorders. Curr Opin Neurol. 2006 Apr;19(2):135-40. doi: ... recessive lissencephaly with cerebellar hypoplasia is associated with ...
  5. ... symptoms. HRAS This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
  6. ... FOXL2 This condition is typically inherited in an autosomal dominant pattern, which means one copy of the altered ...
  7. ... syndrome. TCF4 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...