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Results 1 - 10 of 16 for neurofibroma OR neurofibromatosis
  1. Neurofibromatosis type 2 
    Neurofibromatosis type 2 is a disorder characterized by the growth of noncancerous tumors in the nervous system. The most common tumors associated with neurofibromatosis ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2 - Genetics
  2. Neurofibromatosis type 1 
    Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of ... Beginning in early childhood, almost all people with neurofibromatosis type 1 have multiple café-au-lait spots, ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  3. NF1 gene 
    ... More than 1,000 NF1 mutations that cause neurofibromatosis type 1 have been identified. Most of these ... experience fatigue, fever, and easy bleeding or bruising. Neurofibromatosis Type 1 Protein Neurofibromatosis-related protein NF-1 ...
    https://medlineplus.gov/genetics/gene/nf1 - Genetics
  4. Schwannomatosis 
    ... is usually considered to be a form of neurofibromatosis, which is a group of disorders characterized by ... nervous system. The other two recognized forms of neurofibromatosis are neurofibromatosis type 1 and neurofibromatosis type 2. ...
    https://medlineplus.gov/genetics/condition/schwannomatosis - Genetics
  5. NF2 gene 
    ... NF2 gene have been identified in people with neurofibromatosis type 2, a disorder characterized by the growth ... These tumors arise from Schwann cells. People with neurofibromatosis type 2 can also develop other nervous system ...
    https://medlineplus.gov/genetics/gene/nf2 - Genetics
  6. Legius syndrome 
    ... syndrome also occur in a similar disorder called neurofibromatosis type 1. It can be difficult to tell ... of Legius syndrome are similar to those of neurofibromatosis type 1. Mutations in the SPRED1 gene cause ...
    https://medlineplus.gov/genetics/condition/legius-syndrome - Genetics
  7. Constitutional mismatch repair deficiency syndrome 
    ... to those that occur in a condition called neurofibromatosis type 1. These features include changes in skin ... with CMMRD syndrome will develop a feature of neurofibromatosis type 1 called Lisch nodules, which are benign ...
    https://medlineplus.gov/...ional-mismatch-repair-deficiency-syndrome - Genetics
  8. MSH6 gene 
    ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are ...
    https://medlineplus.gov/genetics/gene/msh6 - Genetics
  9. MSH2 gene 
    ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are ...
    https://medlineplus.gov/genetics/gene/msh2 - Genetics
  10. PMS2 gene 
    ... to those that occur in a condition called neurofibromatosis type 1.Individuals with CMMRD syndrome inherit two ... syndrome.It is thought that the features of neurofibromatosis type 1 in people with CMMRD syndrome are ...
    https://medlineplus.gov/genetics/gene/pms2 - Genetics
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