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Results 1 - 10 of 16 for Unknown inheritance
  1. GHR gene 
    ... and non-genetic factors, some of which are unknown, influence how tall a person will be. GH receptor GHBP GHR_HUMAN growth hormone ...
    https://medlineplus.gov/genetics/gene/ghr - Genetics
  2. FAM83H gene 
    ... enamel, although its role in this process is unknown. At least 20 mutations in the FAM83H gene have been found in an autosomal dominant form of a disorder of tooth development called amelogenesis imperfecta. Autosomal dominant inheritance means that one copy of the FAM83H gene ...
    https://medlineplus.gov/genetics/gene/fam83h - Genetics
  3. IDH1 gene 
    ... determines the type of cell an immature cell will ultimately become (cell fate determination). Instead of becoming normal mature cells, immature blood cells with somatic IDH1 gene mutations divide uncontrollably, leading to CN-AML. It is unknown why somatic IDH1 gene mutations can result in ...
    https://medlineplus.gov/genetics/gene/idh1 - Genetics
  4. SGCE gene 
    ... involuntary movements characteristic of myoclonus-dystonia. It is unknown ... their mothers will develop features of myoclonus-dystonia. It is unclear ...
    https://medlineplus.gov/genetics/gene/sgce - Genetics
  5. HTRA1 gene 
    ... related to tumor progression, the risk that cancer will spread (metastasize) to other parts of ... ARMD7 HtrA HTRA1_HUMAN IGFBP5-protease L56 ORF480 ...
    https://medlineplus.gov/genetics/gene/htra1 - Genetics
  6. AKT1 gene 
    ... blocks (nucleotides) in the AKT1 gene. It is unknown whether the genetic changes have an effect on ...
    https://medlineplus.gov/genetics/gene/akt1 - Genetics
  7. PIK3CA gene 
    ... blood vessel, skin, and bone abnormalities. It is unknown whether individuals with these disorders have an elevated ...
    https://medlineplus.gov/genetics/gene/pik3ca - Genetics
  8. CDH1 gene 
    ... craniofacial development, leading to orofacial clefting. It is unknown why some people with orofacial clefting caused by ...
    https://medlineplus.gov/genetics/gene/cdh1 - Genetics
  9. RBM8A gene 
    ... the development of certain tissues, but it is unknown how it causes the specific signs and symptoms ... Newbury-Ecob R, Ouwehand WH, Ghevaert C. Compound inheritance of a low-frequency regulatory SNP and a ...
    https://medlineplus.gov/genetics/gene/rbm8a - Genetics
  10. FOXL2 gene 
    ... The function of this poly(A) tract is unknown.The FOXL2 protein is active in multiple tissues, ... difficult to predict the type of BPES that will result from the many FOXL2 gene mutations. However, ...
    https://medlineplus.gov/genetics/gene/foxl2 - Genetics
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