About: Neurofibromatosis   Sponge Permalink

An Entity of Type : owl:Thing, within Data Space : 134.155.108.49:8890 associated with source dataset(s)

Neurofibromatosis is any of a number of distinct genetic conditions that result in a high probability of tumor formation. However, all the conditions are caused by inheriting the single defective gene from a parent with the condition. However, in any given patient, the disease can be of varying severity due to the expression of other related genes. They fall into three categories:

AttributesValues
rdfs:label
  • Neurofibromatosis
rdfs:comment
  • Neurofibromatosis is any of a number of distinct genetic conditions that result in a high probability of tumor formation. However, all the conditions are caused by inheriting the single defective gene from a parent with the condition. However, in any given patient, the disease can be of varying severity due to the expression of other related genes. They fall into three categories:
sameAs
dcterms:subject
symptom
  • Uncontrolled growth of tumors
dbkwik:house/prope...iPageUsesTemplate
Name
  • Neurofibromatosis
Type
Cause
  • Fault in any of a number of genes
abstract
  • Neurofibromatosis is any of a number of distinct genetic conditions that result in a high probability of tumor formation. However, all the conditions are caused by inheriting the single defective gene from a parent with the condition. However, in any given patient, the disease can be of varying severity due to the expression of other related genes. They fall into three categories: * Type I – the tumors are generally benign, but can compress nerves and other tissues * Type II – where the tumors form around the acoustic nerves, leading to hearing loss * Schwannomatosis – where painful schwannomas grow around several different types of nerves
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