| dbo:description
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- مرض من الأمراض (ar)
- tipo de enfermedad (es)
- наследственное заболевание (ru)
- type of neurofibromatosis disease (en)
- autosomal dominante Multiorgan-Erkrankung (de)
- malattia genetica autosomica dominante (it)
- maladie monogénique neurodéveloppementale, caractérisée par des symptômes multisystémiques (fr)
- ଏହି ରୋଗରେ ସ୍ନାୟୁ ଅର୍ବୁଦ (ନ୍ୟୁରୋଫାଇବ୍ରୋମାସ) ସୃଷ୍ଟି ହୁଏ । (or)
- людська спадкова хвороба (uk)
- genetische aandoening, veroorzaakt door een mutatie in het gen voor het eiwit neurofibromine (nl)
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- Main symptoms of neurofibromatosis type I. (en)
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- 237.710000 (xsd:double)
- (en)
- Q85.0 (en)
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- Neurofibromatosis type 1 (en)
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- Neurofibromatosis type I (en)
- ورم عصبي ليفي من النوع الأول (ar)
- Neurofibromatosi tipus I (ca)
- Νευροϊνωμάτωση 1 (el)
- Neurofibromatose Typ 1 (de)
- Neurofibromatosis tipo 1 (es)
- I motako neurofibromatosi (eu)
- Neurofibromatose de type I (fr)
- 神経線維腫症1型 (ja)
- Neurofibromatosi di tipo 1 (it)
- Ziekte van Von Recklinghausen (nl)
- Neurofibromatose tipo I (pt)
- Nerwiakowłókniakowatość typu 1 (pl)
- Нейрофиброматоз I типа (ru)
- Нейрофіброматоз І типу (uk)
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- Neurofibromatosis type 1 (en)
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