Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q7616509> ?p ?o }
- Q7616509 subject Q6584894.
- Q7616509 subject Q8367812.
- Q7616509 subject Q8616888.
- Q7616509 subject Q8672688.
- Q7616509 abstract "Template:ForNeurofibromatosis type I (NF-1) is a tumor disorder that is caused by the mutation of a gene on chromosome 17 that is responsible for control of cell division. NF-1 causes tumors along the nervous system and can grow anywhere on the body. NF-1 is one of the most common genetic disorders and is not limited to any person's race or sex. Currently (2015), there are at least 100,000 people in the U.S. and about 150,000 people in the UK who have been diagnosed with NF. Common symptoms of NF-1 include brownish-red spots in the colored part of the eye called Lisch nodules, benign skin tumors called neurofibromas, and larger benign tumors of nerves called plexiform neurofibromas, scoliosis (curvature of the spine), learning disabilities, vision disorders, Mental Disabilities, Multiple café au lait spots and epilepsy.NF-1 was formerly known as von Recklinghausen disease after the researcher (Friedrich Daniel von Recklinghausen) who first documented the disorder.NF-1 is an age specific disease most signs of NF-1 are visible after birth during infancy but many symptoms of NF-1 occur as the person ages, and has hormonal changes.NF-1 is not to be confused with Proteus syndrome. NF-1 is a developmental syndrome caused by germline mutations in neurofibromin, a gene that is involved in the RAS pathway (RASopathy). In diagnosis it may also be confused with Legius syndrome.".
- Q7616509 icd10 "Q85.0(ILDSQ85.010)".
- Q7616509 icd9 "237.71".
- Q7616509 meshId "D009456".
- Q7616509 omim "162200".
- Q7616509 thumbnail NF-1-Tache_cafe-au-lait.jpg?width=300.
- Q7616509 wikiPageExternalLink NBK1109.
- Q7616509 wikiPageExternalLink nfcenter.wustl.edu.
- Q7616509 wikiPageExternalLink nf-clinical-trials.
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