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Myopia "19," autosomal dominant
- ... AUTOSOMAL DOMINANT; MYP15 MYOPIA 20, AUTOSOMAL DOMINANT; MYP20 MYOPIA 19, AUTOSOMAL DOMINANT; MYP19 PubMed Cheng CY, Schache M, Ikram MK, ...
- ... 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 ...
- Williams Syndrome (Genetic and Rare Diseases Information Center)Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
- ... 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 ...
- ... symptoms. HRAS This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... FOXL2 This condition is typically inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... syndrome. TCF4 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...