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- Neurofibromatosis_type_II abstract "Neurofibromatosis Type II (or "MISME Syndrome", for "Multiple Inherited Schwannomas, Meningiomas, and Ependymomas") is an inherited disease. The main manifestation of the disease is the development of symmetric, non-malignant brain tumors in the region of the cranial nerve VIII, which is the "auditory-vestibular nerve" that transmits sensory information from the inner ear to the brain. Most people with this condition also experience visual problems. NF II is caused by mutations of the "Merlin" gene, which seems to influence the form and movement of cells. The principal treatments consist of neurosurgical removal of the tumors and surgical treatment of the eye lesions. The underlying disorder does not have any therapy due to the cell function caused by the genetic mutation.".
- Neurofibromatosis_type_II diseasesdb "8960".
- Neurofibromatosis_type_II emedicineSubject "neuro".
- Neurofibromatosis_type_II emedicineTopic "496".
- Neurofibromatosis_type_II icd10 "D33, Q85.0 (ILDS Q85.020)".
- Neurofibromatosis_type_II icd9 "237.72".
- Neurofibromatosis_type_II medlineplus "000795".
- Neurofibromatosis_type_II meshId "D016518".
- Neurofibromatosis_type_II omim "101000".
- Neurofibromatosis_type_II thumbnail Schwannoma_-_Antoni_A_and_B_-_very_high_mag.jpg?width=300.
- Neurofibromatosis_type_II wikiPageExternalLink nfcenter.wustl.edu.
- Neurofibromatosis_type_II wikiPageExternalLink nf-clinical-trials.
- Neurofibromatosis_type_II wikiPageExternalLink www.advocurenf2.org.
- Neurofibromatosis_type_II wikiPageExternalLink approaches.htm.
- Neurofibromatosis_type_II wikiPageExternalLink www.ctf.org.
- Neurofibromatosis_type_II wikiPageExternalLink www.hei.org.
- Neurofibromatosis_type_II wikiPageExternalLink NBK1201.
- Neurofibromatosis_type_II wikiPageExternalLink www.neuroguide.com.
- Neurofibromatosis_type_II wikiPageExternalLink index.php.
- Neurofibromatosis_type_II wikiPageExternalLink www.nfkontakt.be.
- Neurofibromatosis_type_II wikiPageExternalLink www.sfn.org.
- Neurofibromatosis_type_II wikiPageID "2792071".
- Neurofibromatosis_type_II wikiPageRevisionID "592630754".
- Neurofibromatosis_type_II caption "Micrograph of a schwannoma, a tumor seen in neurofibromatosis type II. HPS stain.".
- Neurofibromatosis_type_II diseasesdb "8960".
- Neurofibromatosis_type_II emedicinesubj "neuro".
- Neurofibromatosis_type_II emedicinetopic "496".
- Neurofibromatosis_type_II genereviewsname "Neurofibromatosis 2".
- Neurofibromatosis_type_II genereviewsnbk "NBK1201".
- Neurofibromatosis_type_II hasPhotoCollection Neurofibromatosis_type_II.
- Neurofibromatosis_type_II icd "237.72".
- Neurofibromatosis_type_II icd "D33, Q85.0".
- Neurofibromatosis_type_II medlineplus "795".
- Neurofibromatosis_type_II meshid "D016518".
- Neurofibromatosis_type_II name "Neurofibromatosis type II".
- Neurofibromatosis_type_II omim "101000".
- Neurofibromatosis_type_II wordnet_type synset-disease-noun-1.
- Neurofibromatosis_type_II subject Category:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Neurofibromatosis_type_II subject Category:Neurological_disorders.
- Neurofibromatosis_type_II subject Category:Neurosurgery.
- Neurofibromatosis_type_II type Abstraction100002137.
- Neurofibromatosis_type_II type Attribute100024264.
- Neurofibromatosis_type_II type Condition113920835.
- Neurofibromatosis_type_II type DeficienciesOfIntracellularSignalingPeptidesAndProteins.
- Neurofibromatosis_type_II type Disease114070360.
- Neurofibromatosis_type_II type Disorder114052403.
- Neurofibromatosis_type_II type IllHealth114052046.
- Neurofibromatosis_type_II type Illness114061805.
- Neurofibromatosis_type_II type Lack114449405.
- Neurofibromatosis_type_II type Need114449126.
- Neurofibromatosis_type_II type NervousDisorder114084880.
- Neurofibromatosis_type_II type NeurologicalDisorders.
- Neurofibromatosis_type_II type PathologicalState114051917.
- Neurofibromatosis_type_II type PhysicalCondition114034177.
- Neurofibromatosis_type_II type State100024720.
- Neurofibromatosis_type_II type Disease.
- Neurofibromatosis_type_II type AilmentCondition.
- Neurofibromatosis_type_II type Situation.
- Neurofibromatosis_type_II comment "Neurofibromatosis Type II (or "MISME Syndrome", for "Multiple Inherited Schwannomas, Meningiomas, and Ependymomas") is an inherited disease. The main manifestation of the disease is the development of symmetric, non-malignant brain tumors in the region of the cranial nerve VIII, which is the "auditory-vestibular nerve" that transmits sensory information from the inner ear to the brain. Most people with this condition also experience visual problems.".
- Neurofibromatosis_type_II label "Nerwiakowłókniakowatość typu 2".
- Neurofibromatosis_type_II label "Neurofibromatose Typ 2".
- Neurofibromatosis_type_II label "Neurofibromatose de type II".
- Neurofibromatosis_type_II label "Neurofibromatosi di tipo 2".
- Neurofibromatosis_type_II label "Neurofibromatosis type II".
- Neurofibromatosis_type_II label "Нейрофиброматоз II типа".
- Neurofibromatosis_type_II label "الورم العصبي الليفي من النوع الثاني".
- Neurofibromatosis_type_II label "神経線維腫症2型".
- Neurofibromatosis_type_II sameAs Neurofibromatose_Typ_2.
- Neurofibromatosis_type_II sameAs Neurofibromatose_de_type_II.
- Neurofibromatosis_type_II sameAs Neurofibromatosi_di_tipo_2.
- Neurofibromatosis_type_II sameAs 神経線維腫症2型.
- Neurofibromatosis_type_II sameAs Nerwiakowłókniakowatość_typu_2.
- Neurofibromatosis_type_II sameAs m.082y40.
- Neurofibromatosis_type_II sameAs Q1935832.
- Neurofibromatosis_type_II sameAs Q1935832.
- Neurofibromatosis_type_II sameAs Neurofibromatosis_type_II.
- Neurofibromatosis_type_II wasDerivedFrom Neurofibromatosis_type_II?oldid=592630754.
- Neurofibromatosis_type_II depiction Schwannoma_-_Antoni_A_and_B_-_very_high_mag.jpg.
- Neurofibromatosis_type_II isPrimaryTopicOf Neurofibromatosis_type_II.
- Neurofibromatosis_type_II name "Neurofibromatosis type II".